BENGALURU · FULLTIME
Medical Writer

Quanticate
Bengaluru · onsite · Posted 3d ago
Sourced from
Undisclosed2–5 yrsfulltimeBengaluru
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Section · 01
About this role
Roles and Responsibilities :
- Develop high-quality clinical study reports, protocols, and other documentation for pharmaceutical companies.
- Collaborate with cross-functional teams to ensure accurate and timely delivery of medical writing projects.
- Conduct research on various diseases and conditions to stay up-to-date on industry trends and developments.
- Ensure compliance with regulatory requirements and company standards throughout the medical writing process.
Job Requirements :
- 2-5 years of experience in medical writing or a related field (e.g., clinical trials).
- Strong understanding of clinical study design, conduct, and reporting principles.
- Excellent written communication skills with ability to adapt tone and style according to audience needs.
- Ability to work independently as well as part of a team.
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Section · 02
Skills
Protocol Writingmedical writingclinical study report
Section · Company
About Quanticate

Quanticate
Pharma
51
employees
1994
32 years old
Bangalore/Bengaluru, Karnataka
India
₹7.4L PA avg
Avg at Quanticate
About
Quanticate operates as a prominent data-centric CRO, specializing in biostatistics and pharmacovigilance for pharmaceutical and biopharmaceutical clients.
Industries
PharmaBiotech & Life sciences
Employee ratings
10 reviews
3.8/ 5
Culture
3.9
Career growth
3.1
Work-life
4.2
Employees rate it well for
Work-Life Balance41Company Culture38
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