Are you a life sciences graduate with a passion for scientific communication? Syngene International Ltd., a leading global contract research organization (CRO), is hiring a Medical Writer in Bangalore, Karnataka. With a legacy since 1993, Syngene collaborates with industry giants like Bristol-Myers Squibb and Merck KGaA, offering innovative solutions in pharmaceutical and biotechnology research. This role is perfect for professionals with 2-4 years of experience in medical writing, eager to contribute to clinical research and regulatory submissions in a dynamic, innovation-driven environment.
Key Responsibilities
As a Medical Writer at Syngene, you will play a pivotal role in creating high-quality clinical and scientific documents for regulatory submissions. Your responsibilities include:
- Drafting Clinical Documents: Independently develop and finalize bioanalytical reports, Clinical Study Reports (CSRs), and eCTD modules across various therapeutic areas and clinical research phases.
- Collaboration: Work closely with internal and external clients to ensure effective communication and operational excellence.
- Project Management: Manage medical writing and review processes to deliver quality projects within agreed timelines.
- Regulatory Compliance: Adhere to regulatory guidelines, department SOPs, and client style guides for all deliverables.
- Quality Control: Perform and respond to documented quality control (QC) checks on medical writing deliverables.
- Literature Reviews: Conduct literature searches to gather background information for scientific content development.
- Additional Duties: Perform other tasks as assigned by the supervisor to support team objectives.
Qualifications and Skills
To excel in this role, candidates should meet the following requirements:
- Educational Background:
- Graduate or Master’s degree in Life Sciences (e.g., Biology, Biotechnology, Pharmacy).
- Experience:
- 2-4 years of experience in medical writing, preferably in clinical research or regulatory writing.
- Technical Skills:
- Strong ability to comprehend and communicate scientific information.
- Good understanding of clinical research processes and regulatory requirements.
- Proficiency in MS Word, PowerPoint, and other relevant software.
- Behavioral Skills:
- Excellent communication and time management skills.
- Quick learner with adaptability to changing priorities.
- Professionalism in client interactions and teamwork.
- Additional Requirements:
- Willingness to attend training on environment, health, and safety (EHS) measures.
Benefits of Working at Syngene
Joining Syngene offers numerous advantages for career growth and professional development:
- Global Exposure: Work with world-renowned clients in pharmaceuticals, biotechnology, and other industries.
- Innovative Culture: Be part of a 4240-strong team of scientists driven by a passion for solving complex scientific challenges.
- Career Development: Access opportunities to enhance your skills in clinical research and medical writing.
- Equal Opportunity Employer: Syngene is committed to diversity, providing equal employment opportunities and reasonable accommodations for individuals with disabilities.
