Job Opportunity: Medical Writer (Remote) at Clinibi
Job Summary:
Clinibi is currently seeking motivated and detail-oriented individuals to join our team as Medical Writers. This is an excellent remote-work opportunity designed for freshers and early-career professionals looking to launch a career in clinical research and regulatory documentation. You will play a vital role in drafting essential regulatory documents, helping to ensure that pharmaceutical and clinical information is communicated accurately and in compliance with global standards.
Job Overview
- Company: Clinibi
- Role: Medical Writer / Regulatory Writer
- Experience: 0–1 Years (Freshers are encouraged to apply)
- Salary: ₹2.5 – ₹4 LPA
- Location: Remote (Work From Home)
- Positions Available: 11
- Employment Type: Full-Time
Responsibilities
As a Medical Writer at Clinibi, you will be responsible for creating, reviewing, and managing documentation that is critical to the drug development lifecycle. Your primary duties will include:
- Document Drafting: Prepare and review Package Inserts (Prescribing Information) and Patient Information Leaflets (PILs).
- Clinical Reporting: Assist in the development of Clinical Study Reports (CSRs).
- Regulatory Submissions: Contribute to the creation of regulatory submission documents, including Clinical Overviews, Clinical Summaries, safety and efficacy summaries, and expert reports.
- Compliance: Ensure all documentation strictly adheres to international regulatory guidelines, including ICH (International Council for Harmonisation) and GCP (Good Clinical Practice).
- Collaboration: Work closely with cross-functional teams in clinical research and regulatory affairs to ensure data accuracy and timely delivery of reports.
Requirements
We are looking for candidates with a strong academic foundation in the life sciences and a passion for technical writing.
Educational Qualifications:
Candidates must hold a degree in one of the following fields:
- B.Pharm / M.Pharm
- B.Sc (Life Sciences, Microbiology, Biotechnology)
- BDS / BAMS / BHMS / BUMS
- Physiotherapy or Nursing
Key Skills:
- Fundamental Knowledge: A strong understanding of the clinical research process, drug development life cycles, and pharmacology.
- Writing Proficiency: Excellent written communication skills in English, with the ability to translate complex medical information into clear, professional documentation.
- Technical Aptitude: Familiarity with medical terminology and a high degree of comfort with scientific literature.
- Attention to Detail: Exceptional analytical skills and a meticulous approach to documentation and record-keeping.
Why Join Clinibi?
This position provides a robust entry point into the high-demand fields of clinical research and healthcare. You will gain hands-on experience with real-world regulatory documents, providing you with a strong professional foundation for future growth in:
- Pharmacovigilance (PV)
- Clinical Data Management (CDM)
- Regulatory Affairs (RA)
Working at Clinibi offers the flexibility of a remote work environment while allowing you to develop specialized skills that are highly valued in the global clinical research organization (CRO) sector.
Benefits
- Remote Work Flexibility: Enjoy a better work-life balance with full-time remote operations.
- Career Advancement: Fast-track your career in one of the most stable and high-growth sectors of the life sciences industry.
- Professional Development: Gain practical, industry-standard experience that will make you a competitive candidate for future global roles.
- Mentorship: Work in a collaborative environment where you can learn from experienced professionals in the regulatory space.
How to Apply
If you are eager to begin your career in medical and regulatory writing, we invite you to apply by submitting your updated resume and cover letter via our official application portal.
[Please visit the official Clinibi careers page or your primary job portal to submit your application directly.]