Parexel Medical Writing Coordinator Freshers Remote
- Clinical Research Career with Parexel – Remote Medical Writing Support Coordinator Opportunity for Freshers
- Company Overview
- Job Role & Responsibilities
- Project Filing & Documentation Management
- Project Support Activities
- Administrative Coordination
- Document Development Support
- Eligibility / Qualifications
- Educational Background
- Skills Required
- Location & Salary
- Application Process
- Frequently Asked Questions (FAQs)
- Is this job suitable for freshers?
- What skills are important for this role?
- Is this a work-from-home opportunity?
- What is the career scope after this role?
- Do I need prior experience?
- Job Summary Table
Clinical Research Career with Parexel – Remote Medical Writing Support Coordinator Opportunity for Freshers
Looking to enter the high-growth clinical research and pharmaceutical industry? Parexel is hiring for the role of Medical Writing Support Coordinator (MWSC) in India (Remote). This is an excellent opportunity for freshers and entry-level candidates with life sciences or healthcare backgrounds to build a strong foundation in medical writing, regulatory documentation, and clinical trial support.
This role sits within the Medical Writing Services (MWS) team and supports Lead Medical Writers across multiple projects. If you’re aiming for a long-term career in clinical research, pharmacovigilance, regulatory affairs, or scientific writing, this position offers strong career progression and global exposure.
Company Overview
Parexel is a globally recognized contract research organization (CRO) that provides advanced clinical research, regulatory consulting, and market access solutions to pharmaceutical, biotechnology, and medical device companies. The company plays a key role in accelerating drug development and improving patient outcomes worldwide.
With a strong presence across global markets, Parexel is known for its scientific expertise, regulatory excellence, and patient-centric approach. The organization actively contributes to bringing innovative therapies to market faster while maintaining strict compliance with global regulatory standards.
Parexel fosters a collaborative and inclusive work culture. Employees benefit from continuous learning opportunities, mentorship programs, and structured career growth plans aligned with global standards. This makes it an ideal workplace for fresh graduates entering the pharmaceutical and clinical research domain.
Job Role & Responsibilities
As a Medical Writing Support Coordinator, you will play a critical support role in clinical documentation and project coordination. Your responsibilities will include:
Project Filing & Documentation Management
- Organize, maintain, and track all project-related documents
- Ensure timely delivery and proper filing of clinical research documentation
- Maintain document version control and compliance with regulatory standards
Project Support Activities
- Assist Medical Writers with project-related tasks and deliverables
- Support client communication and coordination
- Set up and maintain project folders, trackers, and archives
Administrative Coordination
- Schedule meetings and coordinate team discussions
- Record, prepare, and distribute meeting minutes
- Manage project trackers and administrative workflows
Document Development Support
- Prepare quality control (QC) documentation packages
- Support document review processes and submission readiness
- Assist in maintaining inspection-ready documentation
This role gives hands-on exposure to clinical study reports, informed consent forms, pharmacovigilance documentation, and regulatory writing processes.
Eligibility / Qualifications
Candidates with a strong academic background in life sciences or related disciplines are encouraged to apply.
Educational Background
Life Sciences, Pharmacy, Biotechnology, Microbiology, Biochemistry, Clinical Research, Medical Sciences, Healthcare, IT (for documentation systems support)
Skills Required
- Strong written and verbal communication skills
- Attention to detail and ability to manage multiple tasks
- Basic understanding of clinical research and regulatory documentation
- Proficiency in MS Office and document management tools
- Ability to work independently with minimal supervision
- Strong organizational and time management skills
- Confidentiality handling and professional integrity
Freshers with strong academic knowledge and interest in medical writing careers are highly suitable for this role.
Location & Salary
- Location: India (Remote Work Opportunity)
Application Process
Interested candidates can apply directly through the official Parexel careers portal using the link below:
Apply Here: https://jobs.parexel.com/en/job/-/-/877/93492243392?
Frequently Asked Questions (FAQs)
Is this job suitable for freshers?
Yes, this role is ideal for freshers with life sciences or pharmacy backgrounds who want to enter clinical research or medical writing.
What skills are important for this role?
Strong communication, attention to detail, document management skills, and basic clinical research knowledge are essential.
Is this a work-from-home opportunity?
Yes, this is a remote role based in India.
What is the career scope after this role?
You can grow into medical writing, regulatory affairs, pharmacovigilance, or clinical operations roles.
Do I need prior experience?
No prior experience is mandatory, but internships or certifications in clinical research will be an advantage.
Job Summary Table
| Category | Details |
|---|---|
| Company | Parexel |
| Vacancies | Medical Writing Support Coordinator |
| Required Education | Life Sciences, Pharmacy, Biotechnology, Microbiology, Biochemistry, Clinical Research, Medical Sciences, Healthcare, IT |
| Experience | Freshers / Entry-Level |
To apply for this job please visit jobs.parexel.com.
