Senior Program officer- Clinical Trial Network

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About the Organization

Biotechnology Industry Research Assistance Council (BIRAC) is a not-for-profit Section 8, Schedule B, Public Sector Enterprise, set up by Department of Biotechnology (DBT), Government of India as an Interface Agency to strengthen and empower the emerging Biotech enterprise to undertake strategic research and innovation, addressing nationally relevant product development needs.

BIRAC is a industry-academia interface and implements its mandate through a wide range of impact initiatives, be it providing access to risk capital through targeted funding, technology transfer, IP management and handholding schemes that help bring innovation excellence to the biotech firms and make them globally competitive. In its Eight years of existence, BIRAC has initiated several schemes, networks and platforms that help to bridge the existing gaps in the industry-academia Innovation research and facilitate novel, high quality affordable products development through cutting edge technologies. BIRAC has initiated partnerships with several national and global partners to collaborate and deliver the salient features of its mandate.

Job Description

The Sr. Program officer (SPO) will serve in the Program Management Unit for the National Biopharma Mission program at BIRAC. Reporting to the Program Manager, PMU the SPO will get opportunity to contribute to establishment of hospital-based clinical trials networks. The SPO will be responsible for interacting with all the applicants funded under NBM for monitoring the hospital sites in the networks ensuring establishing the systems and processes complying with GCP guidelines. The SPO will also be expected to manage the grants/contracts as part of a team for various projects supported under the Mission.

The appointment shall be under ‘Contract for Service’ initially for a period of three (03) years or Co-terminus with the project, whichever is earlier. The present duration of the project is till June’2025. Renewal of the contract shall depend on the extension of the Project or need for continuance of service, based on satisfactory performance.

Job Responsibilities

• Coordinating with stakeholders involved in establishing clinical trial network and ensuring the quality checks on the disease registry being implemented by the sites.
• Responsibilities for Implementation of the Mission Program which includes Ensuring monitoring of all grantees of your focus area by both technical and financial experts, working closely with the Scientific and Technical Advisory groups for project review and supervising grant management activities.
• Working with Legal and Finance to get all necessary Contracts and Agreements ready.
• Coordination and administration of all aspects of new and ongoing projects including planning and implementation.
• Ensure timely execution of all activities.
• Responsible for supporting the organization investigators meetings, Interaction and Advisory Group Discussion including international conferences and workshops.
• In addition to scientific expertise, the Program officer must also bring in passion, humility, and critical thinking for the unique problems and the questions relevant to BIRAC’s mission.
• Prepare and implement an effective communication and outreach strategy.
• To work and communicate with grantees and key stakeholders.

Education Qualification/Required Skills & Experience

• M.Sc/ M.Pharma/ BDS/MBBS in Life Sciences/Biological Science/Microbiology/ Biochemistry/Biotechnology.
• Diploma or degree in clinical research.

Desirable Qualifications:

MD/MDS/PhD in Life Sciences/Biological Science/Microbiology/Biochemistry/ Biotechnology.

• Demonstrated outstanding written and oral communication skills in positions requiring communications in a broad and diverse audience on a range of complex technical issues.
• Demonstrated strong planning and analytical skills. Excellent interpersonal and negotiation skills.
• Demonstrated capacity and Experience to handle collaboration within an organization and with external partners, as well as ability to work with efficiency and diplomacy as part of a team effort.
• Ability to organize/prioritize work and meet deadlines within a fast-paced environment with multiple and competing demands.
• Proactive and flexible nature with reliable follow-through and attention to detail.
• Ability to work both independently and in a cooperative and collegial fashion.
• Ability and willingness to travel domestic and international.

 Experience:

• Minimum 4 years of experience as a clinical research associate in a company or Not-for profit or as a clinical trial coordinator at a trial site.

For more information please check the Link

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