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LabConnect, LLC
Medical Writer
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What they do
A Medical Writer applies the principles of clinical research in developing clinical trial documents that effectively and clearly describe the research results, product use, and other medical information. Medical writers may also offer writing support to the principal investigators for grant applications and specialized publications.
$83,768 / year median in Tennessee
+6% projected growth
Job Description
Overview LabConnect improves lives by partnering with pharmaceutical and biotech companies, and clinical research organizations (CROs) to accelerate the development of new medicines around the world. We are an independent, global, one-stop-shop focused on delivering Central Laboratory Services that are tailor-made, timely and flexible to meet the evolving study demands of traditional to increasingly complex trials. Additionally, we provide Functional Service Provider (FSP) Solutions, supporting our clients with scientific and technical expertise, acting as an extension of their team, coordinating all laboratory related needs, advising on strategies for lab data collection and providing end-to-end analytical and logistical solutions. The 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.