Manager, Medical Writing - Innovative Medicine R&D
Are you looking for a challenging and rewarding career in the pharmaceutical industry? Do you have a passion for medical writing and a desire to make a difference in patients' lives? Look no further, as Teva Pharmaceutical USA is seeking a highly skilled and motivated Manager of Medical Writing for our Innovative Medicine R&D team.In this role, you will have the opportunity to lead a team of medical writers and collaborate with cross-functional teams to support the development and submission of innovative medicines. Your expertise in medical writing, along with your strong leadership skills, will be crucial in ensuring the quality and accuracy of regulatory documents that are critical to the success of our products.To be successful in this role, you must have a strong understanding of regulatory guidelines and requirements, as well as excellent communication and project management skills. If you are a self-driven individual with a strong sense of accountability and a desire to contribute to the advancement of medicine, we encourage you to apply for this exciting opportunity at Teva Pharmaceutical USA.
- Lead a team of medical writers to ensure the quality and accuracy of regulatory documents for innovative medicines.
- Collaborate with cross-functional teams to support the development and submission of regulatory documents.
- Utilize knowledge of regulatory guidelines and requirements to ensure that all documents comply with industry standards.
- Manage and prioritize multiple projects to meet tight deadlines.
- Oversee the writing, editing, and formatting of various documents, including clinical study reports, protocols, and investigator brochures.
- Provide guidance and mentorship to junior medical writers, ensuring their professional growth and development.
- Review and approve documents for submission to regulatory agencies.
- Coordinate with internal stakeholders to ensure timely and accurate delivery of documents.
- Stay updated on industry trends and regulations to ensure compliance and inform writing practices.
- Implement and maintain standard operating procedures for medical writing activities.
- Act as a subject matter expert for medical writing, providing guidance and support to cross-functional teams.
- Collaborate with regulatory affairs and clinical teams to develop strategies for successful submission of regulatory documents.
- Communicate effectively with key stakeholders, including regulatory agencies and external partners.
- Maintain a high level of attention to detail and accuracy in all written materials.
- Represent the company in a professional and ethical manner.
Advanced Degree In Life Sciences: A Manager, Medical Writing At Teva Pharmaceutical Usa Should Possess An Advanced Degree In A Life Science Field Such As Pharmacology, Biochemistry, Or Molecular Biology. This Will Ensure A Strong Foundation In Medical Knowledge And Terminology.
Extensive Writing Experience: The Ideal Candidate Should Have At Least 5 Years Of Experience In Medical Writing, Preferably In The Pharmaceutical Industry. They Should Have A Proven Track Record Of Successfully Preparing And Submitting Regulatory Documents, Such As Clinical Study Reports And New Drug Applications (Ndas).
Knowledge Of Regulatory Requirements: In Order To Excel In This Role, The Candidate Should Have A Deep Understanding Of Regulatory Requirements And Guidelines, Including Those Set By The Fda And Other Global Regulatory Bodies. This Will Ensure That All Written Materials Are Compliant And Adhere To Industry Standards.
Leadership And Project Management Skills: As A Manager, This Individual Will Be Responsible For Overseeing A Team Of Medical Writers And Coordinating Their Efforts To Ensure Timely And Accurate Delivery Of Documents. Therefore, Strong Leadership And Project Management Skills Are Essential For This Role.
Adaptability And Innovation: At Teva Pharmaceutical Usa, Innovation Is At The Core Of Our R&D Efforts. The Ideal Candidate Should Be Able To Think Creatively And Adapt To Changing Project Priorities And Timelines. This Will Ensure The Successful Completion Of Projects And The Ability To Keep Up With The Fast-Paced And Ever-Changing Pharmaceutical Industry.
Project Management
Data Analysis
Clinical Research
Technical Writing
Team Leadership
Regulatory compliance
Scientific Communication
Publication
Cross-Functional Collaboration
Medical Writing
Pharmaceutical Industry
Fda Guidelines
Communication
Conflict Resolution
Emotional Intelligence
Leadership
Time management
creativity
flexibility
Teamwork
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a Manager, Medical Writing - Innovative Medicine R&D in West Chester, PA, USA is between $95,000 and $140,000 per year. This range may vary depending on the specific company, experience level, and other factors such as bonuses and benefits.
Apply with Video Cover Letter Add a warm greeting to your application and stand out!
Teva Pharmaceutical Industries Ltd., also known as Teva Pharmaceuticals, is an American Israeli pharmaceutical company with dual headquarters in Petah Tikva, Israel and Parsippany, New Jersey, U.S. Teva Pharmaceutical Industries Ltd. engages in the provision of pharmaceutical services. It operates through the following business divisions: Generic, Specialty Medicine, and Over-the-Counter (OTC).
Get interviewed today!
JobzMall is the world‘ s largest video talent marketplace.It‘s ultrafast, fun, and human.
Get Started