Number of posts: One Emoluments: Up to Rs 2,11,200/- Age: 55 years

Minimum Educational Qualification and Experience

Medical professional qualification (MBBS OR BDS or equivalent qualification) from a recognized university with at least 12 years of work experience in clinical project management and/or drug development.

OR

Post graduate degree in a Science or health related discipline with at least 15 years of work experience in clinical project management and/or drug development.

Significant experience of clinical trial or public health project management in a recognized organization /institute (academic clinical trials unit, CRO, pharmaceutical, biotechnology, or device company) leading/directing a clinical study / R&D team.

Job profile

Lead the clinical trial/studies conduct team with overall responsibility for project management including quality monitoring and clinical operations for clinical studies.

A. Leadership and Strategy

·      Support the CDSA Head in the development of overall strategy

·      Lead on drafting relevant policies and standard operating procedures

·      Contribute to developing the clinical trials/studies portfolio

·      Lead on the development of systems/processes for conduct and reporting on clinical trials / studies and medical device portfolio (including mechanisms for prioritizing clinical trials/ studies and for ensuring full cost recovery and income generation).

·      Analyze and formally report data and information on trends related to research sponsorship activities

·      Ensure consistent application of core CDSA policies and operating procedures across the CDSA sponsored trials/ studies portfolio

·      Act as the lead on behalf of CDSA for projects and committees, meeting with internal and external partners (academic and industry collaborations, vendors, sponsors and manufacturers and regulators)

·      Continually review and respond to changes required to shape the infrastructure, functionality and standards of clinical trials/ studies management, including the development and implementation of systems, operating procedures and policies.

·      Effect change and/or ensure dissemination of regulatory effective change management systems are implemented to facilitate the changing clinical trials environment in India and CDSA, in particular the operational implications of new clinical trials and CDSCO/ ICMR regulations and policies.

·      Provide expert support to projects with regards to compliance, policy, sponsorship and high-risk studies

·      Represent CDSA at regulatory inspections and meetings as required

·      Act as a key advisor on, collating project reports and writing position papers as well as advising on “higher risk” studies

·      With the Administrative Manager and Head Regulatory Science and Medical Affairs, oversee and draft Memorandum’s of Understanding (MoU’s) or other documents to outline the delegation of duties from the sponsor office to CDSA and other stakeholders of the projects

·      Actively contribute to or lead on initiatives related to the development of CDSA including resourcing, skills and training, systems and aligned risk assessments and strategies

researchers with regards to trials and “higher” risk studies

·      Ensure the dissemination of information for CDSA staff on the CDSCO/ ICMR Clinical Trials Regulation and its implications, regulatory requirements, research governance and Good Clinical Practice (GCP).

B. Operations Management

·      Oversee the preparation of proposals

·      Participate in business development activities.

·      Participate in clinical review meetings (teleconferences and /or face to face) and document preparation for meetings as required

·      Solicit expert advice, develop collaborative relationship with key experts and investigators

·      Organize meeting with investigators to understand the scope of work

·      Ensure that any relevant Master Services agreement is in place for individual projects

·      Review the Project contract with appropriate functional heads to identify staff necessary for the project team

·      Oversee and ensure implementation of project plan, including all elements listed in the project plan template as appropriate for project (Roles & Responsibilities, Communication Plan, Risk Analysis etc.)

·      Oversee preparation of initial budget for the project

·      Review and provide input for responses to IEC and regulatory agencies

·      Responsible for reviewing study protocols, investigator’s brochure, clinical study reports, IND sections

·      Revise SOPs or suggest process improvements for consideration.

·      May draft new SOPs for review and act as reviewer for Clinical SOPs, as assigned and appropriate.

·      Provide input as necessary to Feasibility Studies, Data Safety Monitoring Committee (DSMC) and other committees, clinical/ product development planning meetings

·      Provide or arrange for project-related training as needed for team members

·      Initiate the project following Best Practices in Project Management

·      Ensure the project is progressing according to quality standards, SOPs, regulations, and guidelines

·      Use project plan as a management tool to record and measure progress, updating as necessary

·      Track resources and actual time spent on each project task for all team members to evaluate project progress and profitability

·      Review metrics reports regularly and follow through on actions required

·      Determine the cause of project overruns, recommend and institute corrective action, with input from functional Primaries

·      Attend and represent project management/ contracted services at internal meetings and investigator meetings

·      Ensure information entered into management system is accurate, and updated on a regular basis

·      Ensure the project is completed within the budget, schedule, and according to contract specifications

·      Provide consulting services to assist in the development of new drugs or devices under the direction of the Head of Organization.

C. Quality Monitoring

·      Work with investigators prior to start of project on incorporation of quality management processes into the scientific and operational design of the trial

·      Develop a monitoring plan with project investigators that is tailored to the specific human subject protection and data integrity risks of the trial

·      Agree predefined quality tolerance limits to identify systematic issues that can impact

·      Be responsible for leading the contracted projects or oversee the studies whenever a designated project lead is assigned to a study.

·      Oversight for quality monitoring as per the approved plans.

·      Visit sites and participating institutes as and when required.

D. Communications

·      Serve as primary contact for the project

·      Communicate to team members the scope of work, timeline and project goals, technical information, and input from client throughout the project

·      Inform team members of any new information or modification of project-related issues which may affect specific responsibilities of team members

·      Work with appropriate Managers on any anticipated need for addition or re-assignment of resources

·      Communicating with study investigators for evaluation of status of participant recruitment and progress to study timelines; supporting safety reporting and IEC submissions; maintaining and reporting metrics for clinical site performance

·      Provide Line Manager with input regarding team members’ performance as needed for employees’ periodic Performance Review

·      Prepare administrative reports and submit to clients as required by the contract exhibit, and other resource reports

·      Communicate fiscal, contractual, resource, deliverable and client- related issues to HoD as appropriate.

E. Training

·   Develop project specific and protocol specific training

·   Provide guidance and operational area training for project team members and staff as required

·  Act as mentor for CPM staff and oversight for their training and development.

· Faculty for training programs conducted by CDSA.

Number of posts: One Emoluments: Up to Rs 1,65,000/- Age: 55 years

Minimum Educational Qualification and Experience

Post graduate degree from a recognized university preferably in Computer application/ Computer science/ Data science or relevant branch with experience of working in a research or healthcare environment and at least 8 years of work experience in clinical data science and/ or data management

OR

Post graduate professional degree preferably in Computer application/ Computer science/ Data science or relevant branch with experience of working in a research or healthcare environment and at least T years of work experience in clinical data science and/ or data management

OR

Graduate degree preferably in Computer science/ Computer application or relevant branch with experience of working in a research or healthcare environment and at least 10 years of work experience in clinical data science and/ or data management

OR

Professional graduate degree preferably in Computer science/ Computer application or relevant branch with experience of working in a research or healthcare environment and at least 9 years of work experience in clinical data science and/ or data management.

·         Experience of working across a range of interventional and observational study designs

·         A comprehensive understanding of ICH Good Clinical Practice, Best practices for clinical data

·         An understanding of clinical trials methodology

·         Experience of Electronic Data Management Systems

Job profile

Lead the Data Science division at CDSA-THSTI. The remit of the Data Science group is to provide clinical database systems development and support for the studies undertaken at the unit, as well as data management support. This includes initiatives to develop and promote best practice in a number of areas including database development, adherence to regulatory requirements, standardization and simplification, data management methods, quality control and assurance. CDSA & THSTI uses a number of different database approaches depending on the needs of the study, including Redcap, a commercial Clinical Data Management System, and bespoke systems- based MS SQL Server with front end development in .NET. The Data Science group also support the study websites, and develop systems to support unit processes.

The primary role of the post holder is to establish, implement and support delivery of high-quality clinical trials/ studies. To ensure data management in CDSA-THSTI is performed to the highest standards, meets GCP and other regulatory requirements.

Leadership and Strategy:

·       Provide leadership and oversee the data science and data management activities in CDSA- THSTI.

·       Lead the development and implementation of data management standards and procedures tailored to ensure that optimal use is made of the clinical data management systems and monitoring tools.

·       Ensure implementation of data management standards and procedures to support study teams and database programmers in the development, deployment and maintenance of study databases.

·       Contribute to developing the clinical trials / studies portfolio

·       Participate in business development activities

·       Serve as a liaison for database development & management functions to all stakeholders — funding agencies, sponsor, investigators, project teams and provide database development and management guidance throughout the life cycle of trials/studies.

·       Develop and support trials with the clinical investigators from grant application stage.

·       Oversee those trials that have successfully received funding through to delivery.

·       Review and improve CDSA-THSTI data management methods to improve the quality, reliability, timeliness and cost effectiveness of clinical trials/ studies at the CDSA_THSTI in collaboration with the IT team, Statisticians and other members of the Trial & Study Management team.

·       Encourage dissemination of best practices in data management to optimise the completeness and validity of study data.

·       Support the CDSA Director and Chief of Clinical Portfolio Management to achieve and maintain the data management standards required of a Clinical Research Unit.

·       Oversee the development and implementation of CDSA-THSTI Policies and Standard Operating Procedures (SOPs) for Data Management processes.

·       Assist the CDSA Director and Chief of Clinical Portfolio Management in the review of relevant contracts and agreements.

Contributing to the database development life cycle

·      Interact with stakeholders to understand the data management needs and develop appropriate solutions

·      Provide oversight and guidance on development process of systems used within the organization (such as cross-study platforms, study websites, portfolio management, etc.)

·      Oversee and provide guidance on procurement of clinical data management and monitoring tools

Review and provide guidance on possible design solutions and evaluate against the project requirements and decide on the most effective design for the application

·      Oversee  the creation  of the software development              environment liaising with server administration as required

Data management support

·      Ensure timely review and approval Data Management plans, and other relevant documentation for CDSA-THSTI trials.

·      Ensure project milestones and deliverables are provided in a timely manner.

·      Ensure data are adequate and available to be shared with internal and external stakeholders, review data sharing requests and oversee data sharing processes.

·      Along with the IT Manager ensure robust measures are in place for data security and confidentiality throughout the study lifecycle, including managing user access to trial databases

·      Advise and assist with data quality assurance and auditing

·      Provide guidance and review the preparation of datasets for analysis including data cleaning and ensuring compliance with the data protection.

·      Maintain a working knowledge of, and assure compliance with, applicable ICH & CDSCO Guidelines, Regulatory Agency requirements, and CDSA SOPs.

Technical Leadership

·      Provide technical leadership for projects as required. This may include, but not be limited to, provide planning information; estimates and task dependencies for budget preparation.

Data quality and methodology

·      Ensure development and implementation of mechanisms for central data monitoring of data in CDSA-THSTI

·      Provide efficient approaches to quality control in the identification of missing data, inconsistencies in the data over time, protocol deviations and reliability of data.

Support the operations and users of applications

·   Work with IT department for applications within the team’s remit as required

·   Provide guidance to team to work with IT department to perform Root Cause Analysis of major incidents and recurring problems with application services and recommend corrective actions

·   Work with IT to perform application upgrades of commercial software in line with CDSA-THSTI

requirements

Standards and training

·  Ensure Good Clinical Practice and Information Governance standards are maintained in relation to data management in clinical studies

·  Support Chief of CPM in the implementation of systems for: resource planning, trial administration and document management, data management and quality assurance.

·  Ensure development of relevant Standard Operation Procedures and Working Practice Documents including the training of staff.

·  Oversee training to CDSA data managers, project managers and CRAs in Clinical data management and monitoring tools.

Number of posts: One Post Emoluments: Up to Rs 1,65,000/- Age: 55 years

Minimum Educational Qualification and Experience

Medical professional qualification (MD OR MBBS or equivalent qualification) from a recognized university with at least 10 years of work experience in clinical research especially in clinical operations (start- up activities), regulatory function, medical affairs including medical monitoring, medical writing, pharmacovigilance and medical coding and systems for adverse event review and reporting, safety reporting and management.

Job profile

Lead the medical and regulatory aspects of clinical trial/studies. Overall responsibility to lead the team on development of protocol, study design, regulatory pathway, medical affairs and safety reporting.

Serve as medical liaison to all stakeholders — funding agencies, investigators, project teams.

Leadership and Strategy:

·  Provide leadership on medical and regulatory aspects of clinical trials and clinical study projects.

·  Participate in business development activities

·  Contribute to drafting policies and standard operating procedures

·  Contribute to developing the clinical trials / studies portfolio

·  Act as a key advisor on regulatory matters, and writing position papers as well as advising on “higher risk” studies.

·  Responsible for dissemination of information for CDSA staff on all CDSCO/ ICMR Clinical Trials Regulation and its implications, regulatory requitrements, research governance and Good Clinical Practice (GCP)

·  Serve as a liaison for medical and regulatory functions to all stakeholders — funding agencies, sponsor, investigators, project teams and provides medical and regulatory guidance throughout the life cycle of trials/studies.

·  Provide guidance and oversees safety management, medical monitoring/coding and medical writing functions.

·  Responsible for start-up activities inclusive of regulatory submission dossiers, wherever applicable, and managing the regulatory compliance of the clinical studies.

·  With the Administrative Manager and Chief of Clinical Portfolio Management, oversee and draft Memorandum’s of Understanding (MoU’s) or other documents to outline the delegation of duties from the sponsor office to CDSA and other stakeholders of the projects

Medical Affairs (50%)

· Provide leadership to clinical trial and clinical study projects on medical and safety aspects.

· Participate in clinical review meetings and document preparation for meetings as required

· Guide the project teams in the preparation and review of study documents like

oclinical protocols, informed consent forms etc.

ointegrated clinical and statistical summary reports,

omeeting presentations

otherapeutic area training material

ojournal articles, and other documents

· Review all documents assigned for scientific/ medically relevant issues including drug safety

· Review and sign off technical documents written with respect to medically relevant matters with particular attention to those relating to drug safety

· DSMB: Develop/ review DSMB charter, support constitution of DSMB for clinical trials, organize and coordinate DSMB meetings

· Provide input as necessary to Feasibility Studies, Data and Safety Monitoring Committees (DSMC) and other committees, clinical/ product development planning meetings

· Act as medical liaison with clients and solicit expert advice, develop collaborative relationship with key experts and investigators

· Assist in the preparation of client proposals

CDSA is involved.

· Train/mentor and provide leadership to the medical monitor(s) and coders assigned to the clinical studies/trials

· Oversee and ensure accurate interpretation of single and or grouped adverse events, serious adverse events, drug effect and attribution of causality, and disease condition

· Oversight / review of clinical narrative reports prepared by the Investigators describing the event; advise on individual participant cases as identified by the study team and identifying queries for the local monitors to complete.

· Ensure compliance with clinical safety and good pharmacovigilance practices and requirements

· Review and provide support in finalizing Periodic Safety Update Reports (PSURs)

· Review and edit CSR for clinical consistency with data and standard of practice

· Review and sign off Data Management listings of safety data (including adverse events, laboratory data, vital signs data, medical history, physical examination, concomitant medication),

· Assist the PI and DSM in establishing the presence or absence of clinically meaningful trends and, if noted, assisting in follow up as appropriate with the project team, sponsor, and Regulatory Authorities

· Review and provide input for AEs (coded), past medical history, concomitant medications or other medical data listings to verify and medically vet clinical data.

· Provide consulting services to assist in the development of new drugs or devices under the direction of the Head of Organization

Regulatory Science (40%)

·  Act as regulatory lead to projects by coordinating regulatory work flow for DCGI and Institutional Ethics Committee submission and approvals, ensuring sufficient regulatory project coverage, providing regulatory support to the team.

·  Review and approve investigator site regulatory package documents (Statement of Investigator, investigator CVs, IRB/IEC approval documentation, consent forms, etc.). Work with the appropriate project team members to resolve queries.

·  Maintain a working knowledge of, and assure compliance with, applicable ICH & CDSCO Guidelines, Regulatory Agency requirements, and CDSA SOPs.

Number of posts: One Post Emoluments: Up to Rs 1,65,000/- Age: 55 years

Minimum Educational Qualification and Experience

· Graduate in any discipline with MBA (Human Resource Management or Finance) or Chartered Accountant or ICWA.

·  Twelve years’ supervisory experience in the relevant field in Central Govt./ State Govt. or autonomous body/ university of Central or State Government.

Job profile

To direct and oversee CDSA’ support services and ensure that all organizational requirements are met relating to operations. The key responsibilities include the following:

Governance

·  Responsible for all governance matters as per the bye-laws / Rules & guidelines of Government of India and those pertaining to the directions issued by the Executive Director or his nominee.

·  Work in the Senior Management Team to improve operational systems, processes and policies to support management reporting, and organizational planning.

·  Ensure that policies and guidance are in place to clearly define responsibilities, processes, delegations and decision-making powers; and fully comply with Institutional requirements.

HR and Gen Administration

· Undertake and be responsible for the development and implementation of appropriate human resource management policies and practices including recruitment, training and development, performance management, employee grievances, annual appraisals and remuneration for all the project staff of the projects undertaken by the extramural Centre.

· Oversee the various functions including resources and outputs, human resource management, facilities, information, and office administration for the Centre.

Finance and Accounts

· Oversee the job of invoicing, accounting, reporting, and other administrative functions to ensure successful execution of grant process

· Reporting of the timely deliverables and expenditure reports and manage financial sustainability and budgets of the extramural Centre

· Development of budgets in line with concept notes and work plans for various clinical trials and studies undertaken by the Centre.

· Responsible for smooth execution of audits by statutory auditors, internal auditors and donor audit (as applicable) including timely and appropriate resolution of observations

Logistics and Contract management

· Responsible for procurement activities in terms of understanding the specifications of the requirement of various projects sanctioned to CDSA as per existing donor budgets and guidelines and procurement processes / policies of the organization. This will include but not limited to clinical site inventory, procurement of IP drug and purchase of clinical trial Insurance.

· Oversee and manage and evaluate logistics operations, liaising with Vendors, suppliers, logistics providers, transportation companies and customers for conduct of workshop and trainings as well travels undertaken for clinical trial research.

· Develop standards for contracts, including presentation of budget, payment terms, general language and provisions. Ensure the contracts executed for the conduct of the clinical trials are following the existing laws governing staff and patient safety, data safety, conflict of interest disclosures and financial terms if any

Site Management

·   Manage relationships, contracts, compliance and interface issues with the different stakeholders including, funding agencies, Sponsors, clinical sites etc. for the sanctioned projects.

·  Conduct due diligence that all project funds are applied for intended purpose

·  Procurement of equipment, IP drug and other items for site.

IT Management

· Procurement of IT equipment, procurement of regular as well high-end software usage, review of the tenders, bid documents and agreements drafted for the procurement of various IT related services, data backup policy and security risks.

· Development of Sop’s for email usage, data back-up, website content and other IT activities Complement the activities of the other departments within the team and provide support wherever required.

Perform other duties as assigned by Executive Director, THSTI or Faculty In- charge, CDSA from time to time for smooth the functioning of the program and to achieve program.

Number of posts: One Post Emoluments: Up to Rs 1,10,000/- Age: 45 years

Medical professional qualification or equivalent (MBBS or BDS or BHMS or BAMS or BPT, etc.)

OR

Master’s degree in Life Sciences OR Pharmacy OR Public Health

OR

Post graduate degree in a health-related discipline.

The candidate should have post qualification experience of at least 5 years in clinical project management and/or clinical trial or public health project management or trial monitoring in a recognized organization/institute (academic clinical trials unit, CRO, pharmaceutical, biotechnology, or device company)

Job profile

This position is responsible for the oversight, management and operational execution of assigned clinical studies. Timely delivery of key tasks, while maintain high standards are key responsibility areas. The program manager will also manage the performance of the project teams(s) working on projects under his/her direction. Mentoring and development of project team is a key outcome area for this role. The program manager will serve as point of contact for the sponsors and build sponsor relationships. The program manager is also responsible for working cross functionally and understanding the implications of project management activities on other groups within organization. In addition, this role may also have the responsibility for the project managing clinical/ non-clinical regulatory trial directly. The program lead will have direct line reports like, but not limited to, project managers and CRA’s.

Number of posts: One post Emoluments: Up to Rs 1,20,000/- Age: 45 years

Minimum Educational Qualification and Experience

MD from a recognized university with at least3 years of work experience.

OR

MBBS OR BDS or MPH from a recognized university with at least 6 years of work experience in clinical research especially in clinical operations, study planning and conduct, regulatory function, medical affairs including medical monitoring, medical writing, pharmacovigilance and medical coding and systems for adverse event review and reporting, safety reporting and management.

Job profile

This position is responsible for taking lead during planning stage of assigned clinical studies and trials, development of grant application in terms of study design, study population, safety reporting, budgeting; protocol development. Timely delivery of key tasks, while maintaining high quality standards are key responsibility areas. The lead Clinical Science will manage the performance of the project team(s) working on projects under his/her direction. Mentoring and development of the project team is a key outcome area for this role. The lead Clinical Science will serve as a point of contact for the sponsors and build sponsor relationships. The lead Clinical Science is also responsible for working cross functionally and understanding the implications of management of clinical science and regulatory affairs activities on other groups within the organization. In addition, this role may also have responsibility for managing the regulatory and medical affairs aspect in clinical/ non- regulatory trial directly. The lead Clinical Science will have direct line reports

The post will work closely with the Director of CDSA and Head of Medical Affairs and Regulatory Science.

Number of posts: One post Emoluments: Up to Rs 1,10,000/- Age: 45 years

Minimum Educational Qualification and Experience

MSc in Statistics

·          Minimum 3 years’ experience in handling/analysing clinical trial & epidemiological study data

·         Experience in using statistical software, especially base, statistics, and graphics; developing statistical analysis plans and statistical methods for protocols; demonstrated use of sample size estimation and power calculation tools/software

·         Knowledge of clinical data management system (paper based and electronic data capturing)

Job profile

Responsible for providing statistical support (design, analysis, and reporting) for large scale, clinical trials/ studies and/or explore methodological improvements in trial design and conduct. The role includes generating randomization schedules, participating in protocol and Statistical Analysis Plan (SAP) development, preparing and reviewing shell tables, listings, and figures, and reviewing case report forms (CRFs), and database structures.

Number of posts: One Post Emoluments: Up to Rs 1,10,000/- Age: 45 years

Minimum Educational Qualification and Experience

Post graduate degree from a recognized university preferably in Computer application/ Computer science/ Data science or relevant branch with experience of working in a research or healthcare environment and at least 6 years of work experience in clinical data science and/ or data management

OR

Post graduate professional degree preferably in Computer application/ Computer science/ Data science or relevant branch with experience of working in a research or healthcare environment and at least 5 years of work experience in clinical data science and/ or data management

OR

Graduate degree preferably in Computer science/ Computer application or relevant branch with experience of working in a research or healthcare environment and at least 8 years of work experience in clinical data science and/ or data management

OR

Professional graduate degree preferably in Computer science/ Computer application or relevant branch with experience of working in a research or healthcare environment and at least T years of work experience in clinical data science and/ or data management

·         Working knowledge in software design and development, techniques, testing and validation methodologies and software documentation.

·         Strong IT skills

·         Experience in Clinical Data Management, Database Administration and Software Development

·         Sound working knowledge of clinical database development and monitoring tools and logics & techniques

·         Demonstrated experience in preparation of Clinical Study Data Management documents

·         Demonstrated experience in software validation and documentation

This position is responsible for taking lead during planning of data management for assigned clinical studies and trials, development of grant application in terms of data management, data protection and data security; budgeting for data management. Timely delivery of key tasks, while maintaining high quality standards are key responsibility areas. The Data Scientist will manage the performance of the data management team(s) working on projects under his/her direction. Mentoring and development of the data management team is a key outcome area for this role. The Data Scientist will serve as a point of contact for the sponsors and build sponsor relationships. The Data Scientist is also responsible for working cross functionally and understanding the implications of data management activities on other groups within the organization. In addition, this role may also have responsibility for data management in clinical/ non- regulatory trial directly. The Data Scientist will have direct line reports like, but not limited to data manager, Quality Analyst, data coordinator and data entry operator.

Number of posts: One Post Emoluments: Up to Rs 1,10,000/- Age: 45 years

Minimum Educational Qualification and Experience

Master’s degree in Life Sciences/ Pharmacy/ Healthcare/ IT/ Education or other related disciplines with 5 years of proven experience in developing and coordinating training programs.

OR

Bachelor’s degree in Life Sciences/ Pharmacy/ Healthcare/ IT or other related disciplines with 8 years of proven experience in developing and coordinating training programs.

Job profile

This position is responsible for developing, management and operational execution of assigned training programs. Timely delivery of key tasks, while maintaining high quality standards are key responsibility areas. The training manager will also manage the performance of the training team(s) working on programs under his/her direction. Mentoring and development of the training team is a key outcome area for this role. The training manager will serve as a point of contact for the sponsors and build sponsor relationships. The training manager will have direct line reports like, but not limited to, training coordinator, etc.

Administrator- Training will have responsibilities that support both department’s vision and purpose. She/he will be working in close coordination with Head Training in meeting various new initiatives and existing programs.

Number of posts: One Post Emoluments: Up to Rs 1,10,000/- Age: 40 years

Minimum Educational Qualification and Experience

MD or MVSc or M. Tech with minimum 2 years’ relevant post qualification research experience

OR

PhD in Life Sciences/ Computational Science/ Bioinformatics/ Genomics from a recognized University with minimum 6 months relevant post qualification research experience.

Job profile

Research and support to the ongoing Big data analysis or next generation DNA sequencing data analysis or Proteomics and metabolomics data analysis.

Number of posts: One post Emoluments: Up to Rs 66,000 /- Age: 30 years

Minimum Educational Qualification and Experience

Bachelors in Human Resource Management/ Life Sciences/ Pharmacy/ IT/ Healthcare or other related disciplines with at least3 years of working knowledge in coordinating training programs

OR

Graduate in any discipline with at least 5 years of working knowledge in coordinating training programs.

Job profile

CDSA’s Training Coordinator will have responsibilities that support both department’s vision and purpose. She/he will be working in close coordination with Head Training and Training Manager in meeting various new initiatives and existing programs. She/he will report to Training Manager.

Number of posts: Four posts Emoluments: Up to Rs 66,000 /- Age: 30 years

Minimum Educational Qualification and Experience

Graduate in Arts or Commerce, or Science or Computer science or Information technology with 3 years’ experience in Central or State Government or autonomous bodies of state or Central Government of India.

Job profile

To provide supervisory support for various administrative functions such as General Administration, HR, Academics, Finance & Accounts, Stores & Purchase, IT Administration Secretarial assistance etc. Some of the principal responsibilities are as below:

· HR and administration

· Account and Finance

· Travel and Procurement

· Information Technology

Number of posts: One position Emoluments: Up to Rs 60,000 /- Age: 30 years

Minimum Educational Qualification and Experience

B Tech in Computer Science and Engineering or relevant branch with 3 years of relevant experience OR

Graduate in any discipline with diploma in Computer application and seven years of experience in system administration, network management, Information technology

Job profile

Responsible for maintaining and administering the CDSA Centre networks including but not limited to the delivery of network planning, design, implementation and optimization of IT services of the Centre.

Number of posts: One position Emoluments: Up to Rs 60,000 /- Age: 30 years

Post graduate degree in science with at least three years of relevant post qualification experience

OR

Post graduate professional degree in relevant branch with at least two years of relevant post qualification work experience

OR

Graduate degree in science with at least five years of relevant post qualification work experience

OR

Professional graduate degree in relevant branch with at least four years of relevant post qualification work experience

OR

Graduate in any discipline with at least eight years’ relevant post qualification work experience

The candidate should have relevant experience in clinical or field work in clinical trials or epidemiological or clinical research.

Job profile

·         Lead a team of field workers/technicians and supervise the operational and technical aspects of implementation of the study specific field/ facility-based procedures

·        Ability to perform field or community-based follow-up visits — telephonic, home -visits, field based anthropometric data collection, home blood sample collection, communication with participants, tracking participants at home

·         Provide input for development of study related material such as community follow-up, telephonic follow-up, home visit SOPs, logs and other study related document

·         Supervise the preparation of lab at site, implementation of laboratory procedures at site

·         Communicate with site lab technicians for tracking laboratory reports of enrolled participant

·         Plans, implements, and maintains data collection systems in support of research protocol; may coordinate the collection of research data.

·         Ensures the smooth and efficient day-to-day operation of clinical and laboratory data collection activities;

·         Act as the primary administrative point of contact for internal research staff and as the principle operational liaison for other research organizations, funding agencies and regulating bodies.

Manage the lab infrastructure, equipment maintenance, stock keeping and indenting reagents as and when required

fee amount