Life Sciences Jobs at IQVIA | Medical Writer Role
Are you looking for Life Sciences Jobs with a globally recognized healthcare and clinical research company? IQVIA Careers has announced an exciting opportunity for a Medical Writer 1 in Bengaluru, India. If you have a Life Sciences background and experience in medical writing, clinical research, or regulatory documentation, this Medical Writer Job offers the chance to work on global projects, collaborate with leading experts, and contribute to the development of innovative healthcare solutions
About IQVIA
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. The company creates intelligent connections that accelerate the development and commercialization of innovative medical treatments, helping improve patient outcomes and population health worldwide. IQVIA combines advanced analytics, technology solutions, and deep scientific expertise to support pharmaceutical, biotechnology, medical device, and healthcare organizations across the globe.
Job Overview
IQVIA Careers is inviting applications for the position of Medical Writer 1 in Bengaluru, India. This hybrid Life Sciences Job is ideal for candidates with a Life Sciences background who have experience in medical writing, clinical research documentation, and regulatory writing. The selected candidate will prepare clinical and regulatory documents, coordinate with customers, manage project timelines, and support drug development activities while working according to IQVIA Standard Operating Procedures (SOPs).
Key Responsibilities
- Act as a Lead Medical Writer on straightforward projects, including simpler documents under standard timelines.
- Prepare assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs), customer requirements, and agreed timelines.
- Confirm project scope, document templates, and specifications.
- Negotiate timelines and discuss or resolve customer comments with senior support when required.
- Keep updated with current medical writing, technical writing, regulatory knowledge, Good Clinical Practice (GCP), and advances in drug development.
- Take a leading role in preparing assigned documents.
- Organize document reviews and communicate directly with customers.
- Manage day-to-day workload by identifying project needs, tracking timelines, and implementing customer requests.
- Keep managers and senior staff informed about project progress and potential issues.
- Attend project team meetings independently or with other writers.
- Participate in or lead comments resolution meetings with external customers.
- Deliver simple presentations to existing customers, such as process overviews during Kick-off meetings.
- Complete project finance activities, including monitoring and forecasting budgeted hours.
- Develop awareness of project budgets, finance principles, and out-of-scope activities.
Qualifications
- Bachelor’s Degree in Life Sciences-related discipline or related field (Required).
- Master’s Degree in Life Sciences-related discipline or related field (Preferred).
- Ph.D. in Life Sciences-related discipline or related field (Preferred).
Experience Required
- Typically requires 1–3 years of prior relevant experience.
- Familiarity with the structure and content requirements of clinical study reports, protocols, and similar documents.
- Good understanding of common statistical methods used in clinical trials and interpretation of results.
- Ability to effectively review a statistical analysis plan and identify deficiencies, errors, and inconsistencies in statistical output (Preferred).
- Ability to integrate, interpret, and summarize data from multiple sources in a clear and concise manner.
- In-depth knowledge of drug development, medical writing, associated regulations, statistical principles, and medical terminology across various therapeutic areas.
Skills Needed
- Excellent written and oral communication skills.
- Strong grammatical and technical writing skills.
- Excellent attention to detail and accuracy.
- Clear, effective, and confident communication.
- Strong collaboration and independent thinking abilities.
- Confidence and maturity in routine medical writing situations.
- Good judgment in seeking input from senior staff.
- Ability to establish and maintain effective working relationships with coworkers, managers, and customers.
- Ability to manage multiple tasks and projects effectively.
- Computer literacy.
If you are searching for Life Sciences Jobs, IQVIA Careers, or Medical Writer Jobs, this opportunity offers an excellent platform to build your career with a global healthcare leader. Candidates with Life Sciences qualifications and relevant medical writing experience are encouraged to apply and become part of IQVIA’s mission to advance healthcare through innovation and scientific excellence.
