4.0 - 8.0 years

6 - 10 Lacs

ahmedabad

Work from Office

Position: Sr. Executive/Assistant Manager - Medical Affairs Department: Medical Affairs Location: Ahmedabad Key Responsibilities Literature search to prepare, review, and finalization of any clinical/non-clinical document. Preparation or review in support of feasibility and related proposal & synopsis. Preparation or review of Investigator Brochure, Investigational Medicinal Product/ Investigational Medical Device Dossier etc. Preparation and review of various clinical trial documents like clinical study protocol / clinical investigation plan, informed consent documents, patient diary cards, clinical study report/clinical investigational report and similar other documents etc. Preparation an...

Posted 1 hour ago

AI Match Score

Apply

Senior Proposal Writer CBM India Trust

7.0 - 10.0 years

12 - 15 Lacs

bengaluru

Work from Office

Position Objective To develop winning proposals, concept notes, and reports for CSR and institutional donors through research, creative and disability-inclusive project design, and proactive donor engagement. Key Roles and Responsibilities A. Proposal Development & Project Design Lead the development of high-quality concept notes and proposals aligned with donor priorities (corporate, institutional, and grant-based). Collaborate with Program and Technical teams to design evidence-based, impactful projects addressing community needs. Develop proposals with strong logical frameworks, detailed budgets, sustainability plans, and measurable outcomes. Maintain an updated repository of organization...

Posted 2 weeks ago

AI Match Score

Apply

Medical Writer II (CSR Safety Narratives) Syneos Health

2.0 - 4.0 years

4 - 8 Lacs

pune

Remote

Role & responsibilities: Main experience in CSR safety narratives writing (authoring, addressing review comments, collaborating with teams) Compiles, writes, edits, and coordinates medical writing deliverables that present scientific information clearly and accurately, and works as a medical writer within and across departments with minimal or moderate supervision. • Completes a variety of documents that may include clinical study protocols and clinical study protocol amendments; clinical study reports; patient narratives; annual reports; investigator brochures; informed consents; annual reports; plain language summaries; periodic safety update reports; journal manuscripts; and abstracts, po...

Posted 3 months ago

AI Match Score

Apply

Regulatory Writer Recruise India Consulting

2.0 - 7.0 years

10 - 20 Lacs

Bengaluru

Hybrid

Minimum Qualification Requirements: Bachelors degree in a scientific, health, communications, technology health related field. Demonstrated experience in technical/ regulatory scientific writing(CSR/Protocol writing/IB) Strong communication and interpersonal skills. Successful completion of writing exercise (a writing exercise is required as part of the candidate evaluation process)

Posted 4 months ago

AI Match Score

Apply

Start Your Job Search Today

Browse through a variety of job opportunities tailored to your skills and preferences. Filter by location, experience, salary, and more to find your perfect fit.