Skip to main content

Pharmacy, Life Sciences Jobs in NBM Program at CDSA - Salary Rs. 1,00,000 pm

Pharma courses


Pharma courses


pharma courses


pharma courses


Life Sciences, Pharmacy Jobs in NBM Program at CDSA

Clinical Development Services Agency (CDSA) is an extramural unit of Translational Health Science and Technology Institute (THSTI) and has been established as a not-for-profit society to provide cost affective, high quality preclinical and clinical product development support services to meet the country’s growing healthcare needs. It will tend enterprises; particularly SMEs involved in new technology innovation and facilitate translation of scientific know-how into viable products.

Post : Program Manager( Public Health) (01 Position)

Program : “NBM Program”

Emoluments (Up to) : Maximum up to Rs. 1,00,000/- per month

Duration : Till May 2022

Location : CDSA Office, Faridabad and NBM, BIRAC office, Delhi, based on the allocated work and/or deliverables

Educational Qualifications & Experience :
Essential qualification :
• MBBS/ BDS/ Alliied Medical degree OR
• Master’s degree / diploma in life sciences, pharmacy, public health, healthcare or other related discipline OR
• Post graduate degree in a health related discipline Essential work experience: 5 or more years of experience in clinical project management and/or clinical trial/ study monitoring
• Experience of clinical trial or public health project management in a recognized organization/institute (academic clinical trials unit, CRO, pharmaceutical, biotechnology, or device company)

Desirable qualification and work experience:
• Postgraduate degree in Public Health
• MD/DNB from a recognized Indian University/ recognized by MCI
• PhD in a health-related discipline
• Demonstrable experience of line management, project management concepts and ability to understand, explain and communicate project concepts using standard tools and templates

• Leadership skills that include the ability to build effective project teams, ability to motivate others, delegation, drive and timely/quality decision making
• Personal qualities that include the ability to gain trust and confidence with a variety of clients, good learning ability, managerial courage, action oriented and resilience in a fast-paced and rapidly changing environment
• Comprehensive understanding of Indian Clinical Trials Regulations, ICH and CDSCO Good Clinical Practice
• Business/ Operational skills that include commitment to quality management and problem solving
• Influencing skills including negotiation and teamwork
• Effective communication skills that include the provision of timely and accurate information to stakeholders, proficient in English, strong written and oral communication skills
• Computer literacy in Word, Excel, PowerPoint, Access or other trial management systems
• Ability to develop and deliver presentations, prepare technical reports and contribute effectively in the manuscripts
• Ability to develop and implement monitoring plans and SOPs
• Ability to make evaluative judgments, remain flexible as projects and priorities change
• Demonstrated ability to prioritize workload in order to meet multiple deadlines
• Ability to work independently with minimal guidance as well as collaboratively within a team setting
• Knowledge of regulations and guidelines pertaining to the conduct of clinical trials/ studies on human subjects

Job Profile
• Responsible for the management and cross-functional coordination of the program and work closely with Project Management Unit (PMU) of National Biopharma Mission (NBM) to develop and maintain the overall project plan and timelines, communicate project expectations to the respective resource / consultant and manage the overall project budget.
• To oversee the management of a portfolio of trials / studies including project management, quality monitoring and/or safety monitoring and guiding the study teams to achieve successful completion of all assigned activities in the program.
• This position may also be required to participate, manage and oversee capacity building at sites for clinical trials as planned by MIU-NBM. This would involve being responsible for completion of all the objectives set out for the sites to ensure they are ready and capable of participating in clinical trials.
• Support the team in the implementation of systems for resource planning, study / trial administration, implementation, oversight monitoring, quality assurance and documentation and record keeping
• Establishment of procedures to ensure adherence to trial protocols and administrative requirements
• Develop project specific and protocol specific training or as requested
• Monitoring the trial progress to ensure compliance with and adherence to the project plan and to identify, evaluate and rectify problems
• Understand the requirements of the various controlling bodies, agencies and frameworks, guiding the project in conforming to those requirements and coordinating any necessary audit processes
• Liaison with Steering Committee and DSMB with a particular view on compliance with Research Governance, Good Clinical Practice, Data Protection and Ethical Requirements
• Work with the Investigators to ensure that the trial is meeting its targets, is producing meaningful output and to predict and plan any changes that warrant requests to changes in protocol, funding, or timelines
• Assists Clinical management with the development, negotiation, and execution of the site contract, budget and payment plan
• Management of the trial budget(s) and maintenance of the accounts
• Development, approval, and distribution of study-related documents including Case Report Forms (CRF’s), study protocols, study manuals, and other study tools to investigational sites and review committees
• Supervise the study start up activities, trial monitoring and reporting
• Manage distribution, collection and tracking of regulatory documentation to ensure compliance with regulatory and project requirements and audit readiness

• Oversight for planning, preparing, and distributing materials for investigator and coordinator meetings, and for study related training
• Work with data management and other departments to track progress, milestones and the challenges
• Works Closely with: Project Team at CDSA, NBM and the site, Sponsors, clinical collaborators, Expert groups / Committee, Regulatory Affairs, Medical Affairs, Data Management, Biostatistics, Laboratory team, key Institute staff on finance, administration, contracts and personnel matters.
• Continually review and respond to changes required to shape the infrastructure, functionality and standards of the program management
• Oversee / Coordinate and draft Memorandum’s of Understanding (MoU’s) or other documents to outline the delegation of duties from the sponsor office to CDSA, NBM and other stakeholders of the projects.
• Support Director CPM for escalations and troubleshooting where issues or concerns are raised by PMU- NBM /researchers with regards to the projects under the program
• Ensure consistent application of core CDSA policies and operating procedures across the NBM program
• Track resources and actual time spent on each project task for all team members to evaluate project progress and CDSA commitment towards NBM
• Communicate to team members the scope of work, timeline and project goals, technical information or update, and input from NBM
• Communicate fiscal, contractual, resource, deliverable and client-related issues to Director CPM as appropriate
• Provide guidance and operational area training for project team members and staff as required
• Act as mentor for study staff and oversight for their training and development.
• Faculty for training programs conducted by CDSA
• Any other assignment with Clinical Portfolio Management team, based on project deliverables or exigencies.

a) This are short-term position and extension will be granted subject to satisfactory performance of the incumbents and tenure of the project for which they are selected. Those appointed to these positions will not have any claim for regularization of their employment.
b) All educational, professional and technical qualification should be from a recognized Board/University.
c) The experience requirement specified above shall be the experience acquired after obtaining the minimum educational qualifications specified for the post.
d) The age limit, qualification, experience and other requirements may be relaxed at the discretion of the competent authority, in case of candidates who are otherwise suitable. In case candidates are not found suitable for the posts notified, they can be offered lower post / lower emoluments on the recommendation of the Selection Committee.
e) Age and other relaxations for direct recruits and departmental candidates:
1. By five years for candidates belonging to SC/ST communities.
2. By three years for candidates belonging to OBC communities.
3. For Persons with Benchmark Disabilities (PWBD) falling under the following categories:
(i) UR - ten years, ii) OBC - 13 years (iii) SC/ST - 15
4. Age is relaxable for Central Government servants up to five years in accordance with the instructions or orders issued by the Central Government, from time-to-time.
5. There is no upper age limit for the Institute employees who are treated as departmental candidates.
f) Age relaxation as per government norms will be provided duly ensuring at least 5 years remaining service for superannuation (60 years).
g) With regard to any provisions not covered in this notification, the bye laws of THSTI / Govt. of India rules / guidelines shall prevail.
h) Canvassing in any form will be a disqualification.

TIME:- 11:00 AM

You are requested to report with all the original and photocopies of following:
i) 02 copies of passport size photo
ii) A comprehensive CV containing details of qualification, positions held, professional experience / distinctions etc.
iii) Matriculation certificate (equivalent to 10th Standard) / Mark sheet)
iv) Intermediate certificate (equivalent to 12th Standard) / Mark sheet)
v) Graduation/Diploma degree certificate / Mark sheet
vi) Post-Graduation degree certificate & Mark sheet (if applicable)
vii) PhD/MD Degree (if applicable)
viii) Relevant experience certificates (if applicable)
ix) Caste / Disability certificate in the format prescribed by the Govt. of India, if applicable.

Apply Online

See All   B.Pharm Alerts   M.Pharm Alerts    Ph.D Alerts   CDSA Alerts

See All   Other Jobs  in our Database

Subscribe to Pharmatutor Job Alerts by Email

Search this website