sr medical writer ( Regulatory)inVentiv Health Clinical SRE, LLC

Job Description :
Job Summary
Serves as a senior medical writer on clinical study or regulatory project teams. Writes, edits, and coordinates content for clinical/regulatory while serving as primary technical contact with the internal team and the client. JOB RESPONSIBILITIES
Mentors and leads less experienced medical writers on complex projects, as necessary.
Acts as lead for assigned writing projects.
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.
Identifies and proposes solutions to resolve issues and questions arising during the writing process, including resolution or escalation as appropriate.
Reviews statistical analysis plans and table/figure/listing specifications for appropriate content, and for grammar, format, and consistency.
Interacts with department head and staff members in data management, biostatistics, regulatory affairs, and medical affairs as necessary to produce writing deliverables.
Serves as peer reviewer on internal review team providing review comments on draft and final documents.
Adheres to established regulatory standards, including but not limited to ICH-E3 guidelines, as well as Company Standard Operating Procedures, 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.
Maintains familiarity with current industry practices and regulatory requirements and guidelines that affect medical writing.
Maintains awareness of budget specifications for assigned projects, working within the budgeted hours and communicating changes to medical writing leadership.
Completes required administrated tasks within the specified timeframes.
Performs other work-related duties as assigned.
Qualifications
Qualifications Requirement
Bachelor of Science degree, preferably Life Science or Medical science qualification.
3- 5 Years of working experience in Regulatory Medical writing
Should have worked on CSR Documents, Protocol, ICF, IB related regulatory documents
Extensive knowledge of English grammar and FDA and ICH regulations and guidelines as well as a familiarity with AMA style guide.
Demonstrated high degree of independence with effective presentation, proofreading, interpersonal, and leadership 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.

Sr Medical Writer (Regulatory)
inVentiv Health Clinical SRE, LLC
Philippines
3-5 years
Not Specified