Job Description

JOB DUTIES RESEARCH CO-ORDINATOR

Protocol development: Collaborate with principal investigators (PIs) and other researchers to design and write trial protocols and supporting documents for clinical studies.

Study setup: Create and organize study files, case report forms (CRFs), and other materials required for the research.

Regulatory submissions: Prepare and submit applications and documents to ethics committees and regulatory bodies to secure necessary approvals.

Sponsor liaison: Act as a central point of contact between the research team, study participants, regulatory bodies, and sponsoring agencies.

Informed consent: Conduct and document the informed consent process, clearly explaining the study's purpose, procedures, risks, and benefits to participants.

Participant monitoring: Schedule and coordinate participant visits, procedures, and follow-ups. Monitor participant adherence to the study protocol and ensure their safety and well-being.

Adverse event reporting: Manage and report any adverse events or unexpected incidents in accordance with regulatory requirements and the study protocol.

Data collection: Gather and record accurate clinical data and observations as required by the study protocol.

Record maintenance: Maintain meticulous and complete research records, including participant charts, consent forms, and regulatory documents.

Quality assurance: Ensure the integrity of all data by adhering to good clinical practices (GCP) and internal quality assurance policies.

Study close-out: Assist with the process of closing out a study, including the final data and document submissions.

Supply management: Maintain an adequate inventory of study supplies, materials, and Ayurvedic products or formulations.

Grant applications: Assist in applying for grants and securing funding for research projects.

Integrative approach: Ensure that the study design, data collection, and analysis incorporate the holistic and individualized principles of Ayurvedic medicine, such as Prakriti (constitution) and Dosha analysis.

Classical text review: Conduct literary and fundamental research based on classical Ayurvedic texts to contribute to study proposals and the development of protocols.

Formulation oversight: Coordinate and document the development, viability, and standardization of Ayurvedic drug formulations used in clinical trials.

Protocol development for therapies: Help develop and document standardized procedures for Ayurvedic therapies and interventions for research purposes.

Job Types: Part-time, Freelance

Pay: ₹8,844.08 - ₹44,054.99 per month

Work Location: In person