Experience
: 3.00 + years
Salary
: Confidential (based on experience)
Shift
: (GMT+05:30) Asia/Kolkata (IST)
Opportunity Type
: Office (Ahmedabad)
Placement Type
: Full time Permanent Position
(*Note: This is a requirement for one of Uplers' client - TatvaCare)What do you need for this opportunity?Must have skills required:CRO, clinical documents, Regulatory documents, Scientific Writing, Medical Writing, Microsoft OfficeTatvaCare is Looking for:
Role Overview Description
Company Overview
Tatvacare is a cutting-edge digital health company based out of Ahmedabad, Bangalore and New Delhi. We provide comprehensive technology solutions that enhance the interactions between patients and doctors, leading to significantly improved health outcomes. With a focus on innovation and service, Tatvacare is poised for rapid growth due to its focused new age digital health tech products, clinical research services including early and late phase clinical studies.
Position Summary
We are seeking a highly skilled and motivated Senior Medical Writer with at least 3+ years of experience in medical writing within the pharmaceutical, CRO, or healthcare industry. The candidate will be responsible for creating, reviewing, and managing a wide range of scientific and regulatory documents, ensuring high-quality deliverables that meet both regulatory and client requirements. The role demands strong writing, analytical, and project management skills, as well as the ability to work collaboratively with cross-functional teams.
Key Responsibilities
- Prepare, review, and edit a variety of scientific and regulatory documents, including clinical study reports, protocols, investigator brochures, patient narratives, informed consent forms, manuscripts, abstracts, and posters.
- Ensure documents comply with ICH-GCP, regulatory guidelines, client specifications, and internal SOPs.
- Collaborate with cross-functional teams including clinical, regulatory, pharmacovigilance, and biostatistics to obtain necessary inputs for document preparation.
- nterpret clinical and scientific data accurately and present it in a clear, concise, and scientifically sound manner.
- Support regulatory submissions by authoring CTD modules and other submission-related documents.
- Conduct thorough literature reviews to support scientific writing and study-related documents.
- Assist in quality control and peer review of documents to ensure accuracy, consistency, and compliance.
- Manage timelines, prioritize tasks, and ensure timely delivery of high-quality documents.
- Participate in project meetings and provide updates on document progress and timelines.
- Contribute to the development and maintenance of templates, style guides, and SOPs for medical writing.
Desired Candidate Profile
- Minimum 3 years of hands-on experience as a medical writer in a CRO, pharmaceutical, or healthcare setting.
- Advanced degree in Life Sciences, Medicine, Pharmacy, or related discipline (PhD/MD/MBBS/MSc preferred).
- Proven track record of writing scientific, clinical, and regulatory documents.
- Excellent command over English language, with strong attention to detail, grammar, and scientific accuracy.
- Familiarity with ICH-GCP, regulatory requirements (FDA, EMA, DCGI), and submission processes.
- Proficiency in MS Office Suite and experience with reference management tools (e.g., EndNote, Mendeley).
- Strong analytical skills with the ability to interpret complex clinical and scientific data.
- Ability to manage multiple projects simultaneously and meet tight deadlines.
- Excellent communication and interpersonal skills to work effectively with cross-functional teams.
- Experience in mentoring or guiding junior medical writers will be an added advantage.
Career Growth
This position offers the opportunity to work on global projects across diverse therapeutic areas, gain exposure to regulatory submissions, and contribute to high-impact scientific publications. The Senior Medical Writer will also have the potential to progress into leadership roles such as Medical Writing Team Lead with responsibilities for mentoring, training, and strategic planning.
How to apply for this opportunity?
- Step 1: Click On Apply! And Register or Login on our portal.
- Step 2: Complete the Screening Form & Upload updated Resume
- Step 3: Increase your chances to get shortlisted & meet the client for the Interview!
About Uplers:
Our goal is to make hiring reliable, simple, and fast. Our role will be to help all our talents find and apply for relevant contractual onsite opportunities and progress in their career. We will support any grievances or challenges you may face during the engagement.(Note: There are many more opportunities apart from this on the portal. Depending on the assessments you clear, you can apply for them as well).So, if you are ready for a new challenge, a great work environment, and an opportunity to take your career to the next level, don't hesitate to apply today. We are waiting for you!
