Require Principal Medical Writer at Syneos Health

Syneos Health™ is an end-to-end, fully integrated biopharmaceutical solutions company that works differently. At Syneos Health, all the disciplines involved in bringing new therapies to market, from clinical to commercial, work together to create customer success. Our unique Biopharmaceutical Acceleration Model delivers value across the small to mid-size to large customer continuum.

Post : Principal Medical Writer (Regulatory)

Job Description :
• Mentors and leads less experienced medical writers on complex projects, as necessary.
• Represents the Medical Writing department on clinical study teams, at conferences, meetings and for presentations to the client regarding a writing project.
• Advises clients and study teams on data presentation and production strategies and on data to ensure that client objectives/expectations are met and quality standards are maintained.
• Develops good working relationships with internal and external colleagues.
• Manages medical writing activities associated with individual studies, coordinating medical writing activities within and across departments with minimal supervision.
• Develops or supports a variety of documents that include but not limited to:
* Clinical study protocols and clinical protocol amendments;
* Clinical study reports;
* Patient narratives;
* Clinical development plans;
* IND submissions and annual reports;
* Integrated summary reports;
* NDA and (e)CTD submissions;
* Investigator brochures, as well as;
* Clinical journal manuscripts, clinical journal abstracts, and client presentations.
• Reviews statistical analysis plans and table/figure/listing specifications for appropriate content, and for grammar, format, and consistency.
• Serves as peer reviewer providing review comments to give maximum clarity of meaning, accuracy relevance and to ensure that client objectives are met and overall quality standards are maintained.
• Adheres to established regulatory standards, including but not limited to ICH-E3 guidelines, as well as company SOPs, client standards, and company and/or client approved templates when completing medical writing projects, on-time and on-budget.
• Performs on-line clinical literature searches, as applicable.
• Continues professional development to keep pace with regulatory guidance and client expectations that affect medical writing and to improve skills.
• Understands budget specifications for assigned projects, working within the budgeted hours and communicating changes to medical writing leadership.
• Completes required administrated tasks within the specified time frames.

Candidate Profile
• Bachelor of Science degree with relevant writing experience with relevant scientific and/or medical knowledge and expertise.
• 8+ years of relevant working experience in Regulatory Medical Writing
• Should have working experience in CSR, Protocol, IBS, Summaries related documents (Must)
• Extensive knowledge of English grammar with a familiarity with AMA style guide.
• Understanding of FDA and ICH regulations and guidelines strongly preferred.
• Demonstrated effective presentation, proofreading, and interpersonal, skills and ensure a team-oriented approach.
• Strong proficiency in Word, Excel, PowerPoint, email, and Internet.
• Ability to demonstrate a familiarity with principles of clinical research and to interpret and present clinical data and other complex information.

Additional Information
Qualification : B.Sc
Location : Hyderabad-Madhapur-Village
Industry Type : Pharma / Healthcare / Clinical research
Functional Area : Regulatory
End Date : 28th February, 2020