Lead Medical Writing
- Employer
- Daiichi Sankyo
- Location
- Basking Ridge, New Jersey, United States
- Start date
- May 21, 2019
View more
- Discipline
- Clinical, Medical Writing
- Required Education
- Masters Degree/MBA
- Position Type
- Full time
- Hotbed
- Pharm Country
Job Details
Daiichi Sankyo, Inc. is the U.S. subsidiary of Daiichi Sankyo, Co., Ltd. The Company currently markets therapies in hypertension, dyslipidemia, diabetes, acute coronary syndrome, thrombotic disorders, stroke risk reduction, opioid-induced constipation, IV iron therapy and metastatic melanoma.
Job Summary
Position is responsible for the preparation of protocols, Investigator Brochures (IBs), Clinical Study Reports (CSRs), clinical sections of the CTD (2.5, 2.7.3, 2.7.4), integrated summaries of efficacy and safety (ISE and ISS), briefing books, and regulatory responses. The position will be responsible for hands-on writing as well as supervision of work performed by CRO/consultant writers on complex projects, and develop medical writing processes and working standards. Documents must be of high quality in terms of scientific content, organization, clarity, accuracy, format and consistency, and adherence to regulatory requirements and company guidelines/styles/processes. In addition, this position has the potential to be a lead writer for protocols, reports, and IBs. As a content expert, this position has a significant understanding of regulatory requirements and ICH guidelines (including E3 and E6), and basic knowledge of document management systems.
Responsibilities
1. Serves as primary author on a wide variety of clinical documents (protocols, reports, investigator brochures, etc), with guidance as needed from functional area experts. Coordinate and control medical writing activities of external writers with regards to company document templates, standards, and processes; Critically review documents produced by external writers for scientific content and alignment with company position, clarity, accuracy, and consistency; Act as liaison between internal and external reviewers and the external writer; Organizes and leads cross-functional meetings to determine timelines and processes for protocol and report development; Addresses QC findings on documents with minimal input from functional area experts
2. Writes high-quality first-draft content with minimal input from functional area experts; Understands clinical data and uses text, tables, and figures as appropriate to accurately and effectively convey key messages; Participate in appropriate development teams and internal strategy and operations meetings
3. Serves as main point of contact with CRO or contract medical writer on complex projects; Ensures that documents written externally conform to company standards and style
4. Develops medical writing processes and working standards; Uses knowledge of document development best practices to continuously improve medical writing SOPs, templates, style guide, etc.
5. Provide independent document quality control services for documents on which the writer has no other role; Check electronically published CSRs for completeness (appendices and required signatures present) and adherence to company's electronic publishing standards before archiving
Qualifications
Education and Experience
- Minimum 2-5 years of experience with a Master's of Science degree or PhD or
- Minimum 5-7 years of experience with a Bachelor's degree
- Regulatory medical writing experience required
Job Title
Lead Medical Writing
City
Basking Ridge
Functional Area
Clinical Development Operations
State
New Jersey
Company
Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and technology.
With more than 100 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and its 15,000 employees around the world draw upon a rich legacy of innovation and a robust pipeline of promising new medicines to help people. In addition to a strong portfolio of medicines for cardiovascular diseases, under the Group’s 2025 Vision to become a “Global Pharma Innovator with Competitive Advantage in Oncology,” Daiichi Sankyo is primarily focused on providing novel therapies in oncology, as well as other research areas centered around rare diseases and immune disorders.
For more information, please visit: www.daiichisankyo.com.
Daiichi Sankyo, Inc., headquartered in Basking Ridge, New Jersey, is a member of the Daiichi Sankyo Group. To learn more about Daiichi Sankyo, Inc., please visit www.dsi.com.
STOCK EXCHANGE: Tokyo Stock Exchange
STOCK SYMBOL: 4568
- Website
- http://www.daiichisankyo.com/
- Phone
- (908) 992-6400
- Location
-
211 Mt. Airy Road
Basking Ridge
New Jersey
07920
United States
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