Medical Writer Job at Catalyst Clinical Research
Looking to advance your career in medical writing and clinical research? Catalyst Clinical Research is hiring a Senior Medical Writer & Evidence Analyst to support regulatory and scientific documentation. This Medical Writer Job at Catalyst Clinical Research in Thiruvananthapuram involves authoring and reviewing high-quality medical writing deliverables. Candidates will work on global regulatory submissions and evidence-based projects. The position offers exposure to diverse therapeutic areas and international guidelines. It is ideal for professionals with strong writing and analytical skills in life sciences.
About the Company:
Catalyst Clinical Research provides customizable solutions to the biopharmaceutical and biotechnology industries. Through Catalyst Oncology and Catalyst Flex, the company offers full-service oncology CRO and multi-therapeutic global services. With a customer-centric approach, innovative technology, and expert teams, Catalyst supports clinical studies worldwide.
Job Details:
- Job Title: Senior Medical Writer & Evidence Analyst
- Industry: Clinical Research / Medical Writing
- Work Type: Full-time
Key Responsibilities:
- Author and review regulatory documents such as CSRs, protocols, IB, and patient narratives in this Medical Writer Job at Catalyst Clinical Research
- Prepare manuscripts, abstracts, posters, and techno-commercial documents
- Ensure scientific accuracy and adherence to quality standards
- Follow ICH and global regulatory guidelines at Catalyst Clinical Research
- Perform quality control, proofreading, and scientific reviews
- Support SOP development and audit readiness in this Job in Thiruvananthapuram
- Collaborate with teams and support department goals
- Adapt writing style based on therapeutic area and client requirements
Educational Requirements for this Medical Writer Job:
- PharmD / MD
- Postgraduate degree in Life Sciences, Medical, or Paramedical fields
Skills Required:
- Strong medical writing and documentation skills
- Knowledge of regulatory guidelines (ICH, GPP)
- Proficiency in Microsoft Office (especially MS Word)
- Excellent written and verbal communication skills
- Analytical and problem-solving abilities
- Ability to manage multiple projects and deadlines
- Flexibility and adaptability in a dynamic work environment
- Strong interpersonal and teamwork skills
Benefits of the Medical Writer Job:
- Opportunity to work with a global clinical research organization
- Exposure to international regulatory and medical writing projects
- Career growth in medical writing and evidence analysis
- Collaborative and innovative work environment
- Opportunity to work across multiple therapeutic areas
- Skill development in regulatory and scientific communication
