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Open nowPosted today

Sr ICF Medical Writing Project Manager

thermofisher2,755 open roles

Where
Remote, Serbia
Work mode
Remote
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Your applicationOpen nowSr ICF Medical Writing Project Managerthermofisher · Remote, Serbia

  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 thermofisher's own form.

The reply lands in your private mailbox

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The clock on this job

Early applications get read.

12.3% of postings close within 7 days. Measured by our own scanner across the market. thermofisher postings stay open a median of 10 days.

Share of postings closed within
  1. 2.1%1 day
  2. 4.5%3 days
  3. 12.3%7 days
  4. 19.3%14 days
  5. 35.6%30 days
  6. 58.1%60 days
This job: posted today

thermofisher median: 10 days open

The posting

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Thermo Fisher Scientific offers impactful work globally, enabling customers to improve health and safety.

We have a vacancy for a Senior ICF Medical Writing Project Manager based in Europe (locations listed).

Discover Impactful Work:

Lead ambitious initiatives that craft the future of clinical research. Your expertise will enable us to deliver flawless Informed Consent Forms (ICFs) and other critical documents, ensuring outstanding quality and compliance.

A day in the Life:

  • Develop project timelines, standards, budgets, and forecasts.
  • Collaborate with cross-functional teams to meet deliverables.
  • Monitor timelines and provide status updates.
  • Identify and resolve client management issues.
  • Ensure compliance with quality processes.

Keys to Success:

  • Proven project management skills.
  • Strong planning and organizational abilities.
  • Excellent interpersonal and communication skills.
  • Ability to work independently and under pressure.

Education

  • Prefer BS/BA in a scientific field with 5 years' experience, or an advanced degree with 3 years' experience.

Experience

  • Experience managing medical writing or clinical projects.
  • Pharmaceutical/CRO industry experience preferred.
  • Advantageous to have experience in regulatory and/or plain language medical writing.

Knowledge, Skills, Abilities

  • Solid project management, budgeting, and forecasting skills.
  • Effective problem-solving and decision-making abilities.
  • Proficient in global and regional regulatory guidelines.

Benefits

We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!

Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

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