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Open nowPosted 78 days ago

Medical Writer

LabConnect23 open roles

Where
Remote - US, 2304 Silverdale Drive, Johnson City, Tennessee, United States of America
Work mode
Remote
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Your applicationOpen nowMedical WriterLabConnect · Remote - US, 2304 Silverdale Drive, Johnson City, Tennessee, United States of America

  1. YouYes, apply to this one.

  2. CV RocketCV written for this posting.

  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

  4. CV RocketApplied on LabConnect's own form.

The reply lands in your private mailbox

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The clock on this job

Early applications get read.

7.8% of postings close within 7 days. Measured by our own scanner across the market.

Share of postings closed within
  1. 1.7%1 day
  2. 3.5%3 days
  3. 7.8%7 days
  4. 14.6%14 days
  5. 34.1%30 days
This job: posted 78 days ago

The posting

  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.

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

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