OverviewThe Medical Writer is responsible for authoring clinical trial and regulatory documents, through independent assignment and oversight as well as engagement within a cross-functional team dynamic. This role requires strategic thinking with exceptional scientific and technical writing skills, excellent communication skills and attention to detail, and the ability to manage and prioritize project load independently.
Essential Duties and Responsibilities- Perform all document authoring steps as outlined by document type and template:
- Author clinical trial and regulatory documents.
- Coordinate quality control of clinical trial and regulatory documents.
- Engage with cross-functional team, as needed.
- Develop accurate, clear and compliant documents as per the project and regulatory requirements.
Education and Experience- Master's Degree or above and at least 5 years' experience in medical writing in the Biotech/Pharmaceutical industry OR Bachelor's degree and at least 8 years' experience in medical writing in the Biotech/Pharmaceutical industry.
- Experience understanding and interpreting data/information and its practical application.
Skills and Ability- Excellent written/oral communication skills and attention to detail.
- Advanced knowledge of scientific/technical writing and editing.
- Strong time and project management skills.
- Strong leadership experience in a team environment.
- Ability to independently prioritize and execute projects in alignment with critical deadlines.
- Industry experience required.
Supervisory Responsibilities: None
Physical Demands:While performing the duties of this job, the occupant is regularly required to:
- Prolonged periods of sitting at a desk and working on a computer.
- Prolonged use of computer and headphones for conference calls.
- Communicate effectively via phone, video, and email.
- Use hands and fingers to operate a computer and other office equipment.
Travel Requirements: Minimal
Join our team and discover how your work can
impact patients' lives around the world!
Some of the Perks our LabConnectors Love:- Financial Security (Base Pay, 401k Match and Possible Annual Bonus Eligibility)
- Health Benefits beginning on date of hire
- PTO plan, plus 11 Paid Company Holidays, and 1 Day to Volunteer in your community
- Short and Long-Term Disability, Life Insurance, and AD&D
- We celebrate our differences, which enriches our culture!
In addition to great perks and challenging work assignments, we invest in our people with career growth opportunities, globally. We believe in a friendly and collaborative environment with open lines of communication. While living out our values of
People First, Quality Focused, Customer Centered, Technology Driven, and
Accountability Always.
