BD Medical Writer Remote Hiring Clinical Writing Role
- BD Hiring Medical Writer (Remote) | 2–4 Years Clinical Writing Experience Required
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities:
- Eligibility / Qualifications
- Educational Background:
- Experience Required:
- Skills Required:
- Location & Salary
- Application Process
- Frequently Asked Questions (FAQs)
- 1. Is this role remote?
- 2. What type of documents will I work on?
- 3. Is medical device experience mandatory?
- 4. What career growth can I expect?
- Summary
BD Hiring Medical Writer (Remote) | 2–4 Years Clinical Writing Experience Required
Looking for a high-growth career in medical writing and clinical research? BD (Becton, Dickinson and Company) is hiring Medical Writers for its Clinical Affairs team. This is a remote opportunity based out of Gurgaon (Haryana), ideal for professionals with 2–4 years of experience in clinical and regulatory medical writing.
This role focuses on clinical evaluation reports, regulatory documentation, and scientific data analysis for medical devices, offering strong exposure to global regulatory submissions and high-value healthcare projects.
Company Overview
BD (Becton, Dickinson and Company) is a leading global medical technology company that develops, manufactures, and sells medical devices, laboratory equipment, and diagnostic products. With a presence in more than 190 countries, BD plays a critical role in advancing healthcare by improving medical discovery, diagnostics, and patient care.
The Interventional Surgery Business Unit operates at the forefront of innovation, supporting clinical development and regulatory approval of advanced medical devices used worldwide.
Job Role & Responsibilities
As a Medical Writer, you will be responsible for creating high-quality clinical and scientific documentation used in regulatory submissions and product development.
Key Responsibilities:
- Prepare, write, and revise clinical documents for global regulatory submissions
- Develop Clinical Evaluation Plans (CEP) and Clinical Evaluation Reports (CER)
- Conduct systematic literature reviews and scientific research using databases like PubMed, Embase, and Ovid
- Analyze and summarize clinical data from trials, real-world evidence, and literature
- Collaborate with cross-functional teams including Regulatory Affairs, Quality, and Product Development
- Ensure documentation complies with regulatory guidelines such as EU MDR and MEDDEV
- Support post-market surveillance reporting and safety evaluations
- Maintain documentation standards as per corporate and regulatory requirements
Eligibility / Qualifications
Educational Background:
B.Pharmacy, M.Pharmacy, Pharm.D, BSc, MSc (Life Sciences, Biotechnology, Microbiology, Biochemistry), MPH, PhD
Experience Required:
- 2–4 years of experience in medical writing or clinical research
- Hands-on experience in writing Clinical Evaluation Reports (CERs)
- Experience with medical device documentation (Class II / Class III preferred)
- Familiarity with regulatory frameworks such as EU MDR, MEDDEV, MDCG, IMDRF
Skills Required:
- Strong scientific writing and analytical skills
- Expertise in literature search tools like PubMed, Embase, Ovid
- Understanding of clinical research methodologies and regulatory requirements
- Excellent English writing and proofreading skills
- Ability to manage multiple projects in a matrix environment
Location & Salary
- Location: Remote (Gurgaon, Haryana base)
- Job Type: Full-time
- Salary: Competitive salary package based on experience
This role offers strong career growth in medical writing, regulatory affairs, and clinical research, which are among the most high-paying and globally in-demand domains in healthcare and life sciences.
Application Process
Interested candidates can apply directly through the official BD careers portal:
Apply Here: https://jobs.bd.com/en/job/-/-/159/92831426720
Candidates are encouraged to apply early as positions in medical writing are highly competitive.
Frequently Asked Questions (FAQs)
1. Is this role remote?
Yes, this is a remote position with a base location in Gurgaon, Haryana.
2. What type of documents will I work on?
You will work on Clinical Evaluation Reports (CERs), Clinical Evaluation Plans (CEPs), regulatory submissions, and post-market surveillance documents.
3. Is medical device experience mandatory?
It is preferred, especially experience with Class II or Class III devices, but related clinical writing experience is also considered.
4. What career growth can I expect?
You can grow into roles such as Senior Medical Writer, Regulatory Writing Specialist, Clinical Scientist, or Global Regulatory Lead.
Summary
| Category | Details |
|---|---|
| Company | BD (Becton, Dickinson and Company) |
| Vacancies | Medical Writer |
| Required Education | B.Pharmacy, M.Pharmacy, Pharm.D, BSc, MSc, MPH, PhD |
| Experience | 2–4 years |
To apply for this job please visit jobs.bd.com.
