⏳ Last Date to Apply: Ongoing / Openings Available
Parexel Senior Medical Writer Recruitment 2026: Apply Online
Senior Medical Writer – FSP
Job Overview
As a Senior Medical Writer at Parexel, your strong scientific knowledge, writing skills, and patient focus effectively communicate complex scientific data to various stakeholders, including regulatory agencies, medical professionals, and the general public. You must be able to collaborate within cross-functional teams to achieve the development of a wide range of clinical research documents, such as model informed consent forms, clinical study reports, pharmacovigilance documents, and more.
We foster a culture of inclusivity, collaboration, and support that empowers our employees to make a meaningful impact on people’s lives. We offer continuous learning from being mentored to job shadowing, job rotation, and stretch assignments, as well as becoming a mentor or leading a team. Your development and promotion are based on global standards and your personal development plan.
Key Job Details
| Company Name | Parexel International |
| Job Role | Senior Medical Writer – FSP |
| Experience | Experienced Professional |
| Salary Range | Competitive & Market Standard |
| Job Type | Private |
| Work Mode | Remote / Hybrid |
| Openings | Multiple |
| Job Location | Hungary / UK / Netherlands (Remote) |
Key Responsibilities
- Develop and maintain clinical and regulatory documents including CTRs, CTPs, protocol amendments, IBs, biomarker reports, and submission documents.
- Manage clinical documents within the Electronic Document Management System (EDMS), including document setup, workflow management, and approvals.
- Establish, communicate, and maintain agreed project timelines in collaboration with trial and project teams.
- Prepare for, facilitate, and document project meetings, kick-off meetings, and trial team meetings as required.
- Coordinate and manage document review cycles, drive alignment on comments, and integrate revisions.
- Initiate, conduct, or oversee quality control activities and complete supporting quality control documentation.
Requirements & Qualifications
- Bachelor’s degree or equivalent combination of education and relevant experience in a life sciences field.
- Knowledge of clinical development documentation processes and regulated working environments.
- Experience working with Electronic Document Management Systems (EDMS) and document lifecycle management processes.
- Strong communication, organization, stakeholder management, and problem-solving skills.
Required Skills
- Strong Medical Writing & Authoring
- Project Coordination & Timeline Management
- Attention to Detail & Quality Control
- Cross-Functional Collaboration
- EDMS & Document Lifecycle Management
About Parexel International
Parexel is a leading global clinical development partner delivering insight-driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and accelerate the delivery of new therapies.
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