Medical Writer Job at Allucent – MD Graduates Apply Now!
An excellent Medical Writer job opportunity is available at Allucent for science and medical graduates seeking to enter regulatory consulting. This role is well-suited for candidates exploring MD jobs and early-career medical writing roles, with potential relevance for professionals searching for jobs in Chennai and similar regulatory hubs.
Job Details:
- Job Position: Medical Writer (Associate-Level Role)
- Company Name: Allucent
- Location: Chennai
About the Company:
Allucent is a global regulatory consulting organization supporting pharmaceutical, biologic, and medical device development. The company offers comprehensive services across regulatory strategy, clinical development, and medical writing, making it an attractive employer for candidates seeking a Medical Writer job, MD jobs, and international regulatory careers.
Qualifications:
Educational Qualifications
- M.S., M.D., or equivalent degree strongly preferred, making this suitable for MD jobs in regulatory writing
Experience Requirements
- ≤ 1 year of directly relevant work experience in drug, biologic, or device development post-degree
- Some medical writing experience is required for this Medical Writer job
Medical Writer Job Description:
The Associate Medical Writer assists in writing, editing, and compiling written deliverables in the disciplines of chemistry, manufacturing, and controls (CMC), nonclinical, clinical, medical, and regulatory for submission to regulatory agencies of Allucent Regulatory Consulting. This Medical Writer job develops skills in scientific discussions regarding the planning, production, and review of written deliverables and is part of the medical writing staff.
Key Responsibilities:
- Assists with writing, editing, and compiling written deliverables in CMC, nonclinical, clinical, medical, and regulatory disciplines for submission to regulatory agencies such as the U.S. Food and Drug Administration
- Contributes to scientific discussions regarding the planning, production, and review of written deliverables as part of this job role
- Develops knowledge of applicable regulatory agency requirements, International Council on Harmonization (ICH) Guidelines, and industry best practices
- Develops knowledge of company templates, requirements, and resources related to the production of written deliverables
Management, Learning & Development
- Applies company policies and procedures to resolve a variety of issues
- Supports continuous learning aligned with long-term MD jobs and regulatory writing careers
Quality Management
- Contributes to the evaluation and improvement of processes and procedures within the Quality Management System
- Follows company policies and standard operating procedures required
Skills Required for a Medical Writer Job:
- Writes, edits, and compiles written deliverables with autonomy commensurate with experience
- Adheres to regulatory practices such as 21 CFR and ICH-E3
- Follows company or sponsor guidelines as directed by the project manager
- Communicates changes in scope or budget to the project manager and medical writing management
- Collaborates with cross-functional teams, including data management, statistics, regulatory strategy, and clinical operations
- Seeks professional development and certifications (RAC, MWA, CMPP, CCRP)
- Proficiency in Word, Excel, and PowerPoint
