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Medical Writer

Planet Pharma

United Kingdom

On-site

GBP 45,000 - 70,000

Full time

5 days ago
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Job summary

Planet Pharma seeks an experienced Medical Writer to join a globally renowned clinical research organisation. The role involves leading the preparation of regulatory submissions and clinical documents, contributing to the development of groundbreaking therapies. The ideal candidate will have strong project management skills and experience in Phase I-III medical writing.

Qualifications

  • Proven experience in Phase I-III protocol and Clinical Study Report (CSR) medical writing.
  • Strong stakeholder management skills.
  • Solid project management and leadership experience.

Responsibilities

  • Lead in authoring high-complexity study-level documents.
  • Prepare regulatory submissions and clinical documents.

Skills

Stakeholder Management
Project Management

Job description

Direct message the job poster from Planet Pharma

Medical Writer – Global Clinical Research Organisation

Planet Pharma is collaborating with a globally renowned clinical research organisation (CRO) to recruit an experienced Medical Writer. This role offers the opportunity to contribute to the preparation of regulatory submissions and other complex clinical documents, playing a key part in bringing innovative therapies to market.

Role Overview:

As a Medical Writer, you will take the lead in authoring high-complexity study-level documents, including:

  • Protocols, Informed Consent Forms (ICFs), Investigator Brochures, and Meeting Packages
  • Clinical Evaluation Plans and Clinical Evaluation Reports
  • Clinical Summaries and Overviews in CTD/eCTD formats for global regulatory submissions

Key Requirements:

We are looking for an experienced medical writer with a strong track record in leading medical writing projects. The ideal candidate will have:

  • Proven experience in Phase I-III protocol and Clinical Study Report (CSR) medical writing
  • Strong stakeholder management skills, working effectively with internal and external teams
  • Solid project management and leadership experience

This is a fantastic opportunity to join a respected CRO, work across diverse therapeutic areas, and play a pivotal role in the development of groundbreaking treatments.

About Planet Pharma:

Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its headquarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.

Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognized by FORBES as the 17th best professional staffing firm and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.

We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.

www.planet-pharma.com

Seniority level
  • Seniority level
    Associate
Employment type
  • Employment type
    Contract
Job function
  • Job function
    Writing/Editing, Science, and Research
  • Industries
    Pharmaceutical Manufacturing and Biotechnology Research

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