Medical Writer

Labcorp Drug Development is seeking a Medical Writer to join our Clinical Pharmacology Services team in the Early Phase division. This is a full-time and permanent position. The Lead Writer is independently responsible for preparing clinical study protocols, clinical study reports (CSRs), and other documents as needed for lower complexity studies.

What to Expect

• Provides support to more experienced writers with the preparation of clinical study protocols, CSRs, and other clinical documents.
• Interpretation of clinical, pharmacokinetic, pharmacodynamic, and statistical results as appropriate.
• Ensure timely delivery of high-quality documents to internal customers and Sponsors.
• Provision of training for Associate Medical Writers and other staff as appropriate.
• Foster excellent working relationships with all internal and external clients with the highest quality of service in a cost-effective manner on time, every time.

​Education / Qualifications

• Minimum of first degree in life sciences (or equivalent); advanced degree (e.g., Ph.D. or Masters) preferred.

​Experience

• Minimum 1-year medical writing experience or 2 years professionally-related experience.
• Excellent command of written and spoken English.
• Good written and verbal communication skills.
• In-depth knowledge of MS Word.
• Good organizational and time management ability.
• Excellent attention to detail.
• Excellent interpersonal skills.
• Scientific or Clinical research experience is desirable.
• Good scientific writing skills.
• Understanding of medical, pharmacokinetic, and statistical principles.