Are you a passionate and detail-oriented Medical Writer looking for a new challenge in the clinical trial industry? Fidelity Health Services is hiring a Medical Writer (Clinical Trial) professional to join their growing team in Mumbai.
✅About the Job
As a Medical Writer (Clinical Trial) at Fidelity Health Services, you will be responsible for writing, reviewing, and editing clinical trial documents, including CSPs, CRFs, ICDs, PIS, IBs, CSRs, manuscripts, and regulatory submissions. You will work closely with internal and external stakeholders to ensure compliance with ICH-GCP and regulatory guidelines.
✅Key Responsibilities
Write, review, and edit clinical trial documents (Phase 2-4)
Develop and maintain clinical trial documents, including CSPs, CRFs, ICDs, PIS, IBs, CSRs, manuscripts, and regulatory submissions
Review literature and ensure compliance with ICH-GCP and regulatory guidelines
Manage documentation, version control, and QC processes
Collaborate with internal and external stakeholders
Support audits, inspections, and development of templates and style guides
✅Requirements
Strong foundation in clinical research documentation and ICH-GCP
Experience in regulatory writing and clinical trial documentation
Excellent writing, editing, and communication skills
Ability to work independently and as part of a team
Strong attention to detail and organisational skills
✅What Fidelity Health Services Offers
Opportunity to work with a leading healthcare company
Collaborative and growth-oriented environment
Competitive compensation and benefits package
Professional development and growth opportunities
State-of-the-art facilities and equipment
✅Why Choose Fidelity Health Services?
We are a leading healthcare company with a strong reputation for excellence
We offer a collaborative and growth-oriented environment that fosters professional development and growth
We provide opportunities for career advancement and learning
We have a strong commitment to quality and compliance
✅Career Growth and Development
At Fidelity Health Services, we’re committed to providing our employees with opportunities for career growth and development. As a Medical Writer (Clinical Trial), you’ll have the opportunity to work on a wide range of projects and develop your skills in areas such as:
Clinical trial documentation and regulatory writing
ICH-GCP and regulatory compliance
Medical writing and editing
Collaboration and communication with internal and external stakeholders
Leadership and management
📬 How to Apply
Ready to take your medical writing career to the next level? 🚀
Send your updated CV to 📧 hrrecruitment@fidelityhs.com
We can’t wait to hear from you! 🙌
✅Frequently Asked Questions
Q: What is the primary responsibility of a Medical Writer (Clinical Trial)?
A: The primary responsibility of a Medical Writer (Clinical Trial) is to write, review, and edit clinical trial documents.
Q: What skills are required for a Medical Writer (Clinical Trial)?
A: A Medical Writer (Clinical Trial) should have strong writing, editing, and communication skills, as well as experience in clinical research documentation and ICH-GCP.
Q: What kind of career growth and development opportunities are available?
A: We offer professional development and growth opportunities, including training and certification programs, leadership development, and opportunities to work on high-profile projects.
Interested
Thank you for showing interest in this opportunity! 🌟
We’re glad to know you found this job post relevant. Please follow the application details mentioned in the post and apply directly through the provided link or company contact. Wishing you the best of luck with your application! 🚀
Interested,
Thank you for showing interest in this opportunity! 🌟
We’re glad to know you found this job post relevant. Please follow the application details mentioned in the post and apply directly through the provided link or company contact. Wishing you the best of luck with your application! 🚀