Build Your Future With a Medical Writer Job at Allucent
If you’re searching for a rewarding medical writer job with global impact, Allucent offers an excellent opportunity to grow your career in regulatory and scientific writing. Whether you are exploring jobs in Chennai or building a future through Allucent careers, this role allows you to contribute to high-quality documentation used in global regulatory submissions. With strong mentorship, learning programs, and collaborative teams, Allucent helps medical writers excel in a fast-evolving life sciences landscape.
Job Details:
- Job Position: Senior Medical Writer
- Location: Chennai
About the Company
Allucent is a global contract research and development organization known for supporting biotech innovation and advancing clinical development worldwide. As part of Allucent careers, professionals get the chance to work with cutting-edge science, regulatory strategies, and industry-leading experts. Whether you’re exploring global opportunities or jobs in Chennai, Allucent offers an inclusive and growth-centered workplace.
Qualifications:
- B.S. in a scientific field required; M.S. or M.D. strongly preferred.
- Up to 1 year of relevant experience in drug, biologic, or device development, including medical writing exposure.
- Strong understanding of scientific principles and regulatory requirements.
- Proficiency with Microsoft Word, Excel, and PowerPoint.
- Excellent written, verbal, and interpersonal communication skills.
- Ability to work effectively with moderate supervision.
- Knowledge of ICH Guidelines and regulatory submission standards.
- Ability to adapt to changing project needs and timelines.
- Interest in certifications such as RAC, MWA, CMPP, or CCRP is an advantage.
Medical Writer Job Description:
This medical writer job at Allucent involves writing, editing, and compiling scientific and regulatory documents across CMC, clinical, nonclinical, and medical domains. The role supports regulatory submissions to agencies such as the U.S. Food and Drug Administration, as well as sponsor use and publication needs. As part of Allucent careers, medical writers contribute to scientific discussions, assist in developing templates, and ensure compliance with global regulatory standards and ICH Guidelines.
Key Responsibilities:
- Write, edit, and compile CMC, clinical, medical, nonclinical, and regulatory documents for submissions and publication.
- Participate in scientific discussions to plan and review written deliverables.
- Develop knowledge of regulatory requirements, ICH Guidelines, and internal templates.
- Conduct literature searches as needed for assigned projects.
- Apply regulatory practices such as 21 CFR, ICH-E3.
- Collaborate with cross-functional teams in a matrix environment.
- Support business development activities within Allucent careers.
- Rare travel; occasional lifting up to 25 pounds may be required.
Skills Required for a Medical Writer Job:
- Ability to independently write, edit, and compile documents based on experience level.
- Awareness of project budgets and contract scope.
- Strong collaboration skills with interdisciplinary teams.
- Ability to contribute to sponsor meetings and scientific discussions.
- Effective literature search capabilities.
- Excellent communication and time-management abilities.
