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Medical Writer - P

Employer
ClinChoice
Location
United Kingdom
Salary
Competitive
Start date
26 Mar 2019
Closing date
25 Apr 2019

View more

Discipline
Medical Communications, Medical Writing
Hours
Part Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Job Details

Description:
Job Title: Medical Writer

Location: United Kingdom

Schedule: Full time, 37.5 hours per week

TalentSource Life Sciences is currently recruiting for an experienced Medical Writer to join one of our partner biopharmaceutical companies based in France. This is a permanent position and we are flexible with the work location, either office based at our office in Stirling or home based. Flexibility to travel to France will be necessary as part of this role.

The successful candidate will be working on studies dedicated to one client.

TalentSource is the division of CROMSOURCE dedicated to flexible staffing solutions. Through us, you will have the opportunity to be integrated into a sponsor-led team, whilst having the continuous support from your TalentSource Line Manager who will work closely with you to support your professional development and growth. For our client-facing positions, you must be confident, be able to drive the role and work autonomously.

Responsibilities:
  • Write and prepare a wide variety of clinical and safety documents from initiation to submission, including (but not limited to) Protocols and Clinical Study Reports (CSRs), summary documents, Risk Management Plans, Clinical Study Summaries and Investigator Brochures.
  • Manage document development to ensure the content produced is prepared to a high standard, meets the agreed timelines and complies with regulatory requirements.
  • Collaborate and interact with team members and stakeholders from a variety of functions to ensure these documents are fit for purpose, while still telling a clear, compelling story.
  • Setting document quality standards, ensuring compliance with internal standards and external requirements.
  • Contribute to the scientific and regulatory strategies.


Education / Qualifications:
  • Bachelor's Degree or equivalent in a relevant scientific field, higher degrees (PhD/MSc) preferred


Experience, Skills & Knowledge:
  • Must have extensive experience in scientific/medical writing
  • Experience authoring Protocols, Clinical Study Reports (CSRs), including narratives.
  • Project management skills, including the ability to consistently achieve multiple tasks and objectives on time
  • Advanced proficient in English (writing and speaking)
  • Excellent written and verbal communication skills. Mastery of the English language, with a comprehensive understanding of English grammar and punctuation.
  • Ability to work effectively in a team environment, establishing strong collaborative relationships.
  • Passion for data interpretation, scientific writing and making meaningful contributions to medicine.


If you have the experience needed for this position, please apply directly to https://www.talentsourcelifesciences.com/job-information/?job-id=Hq00001711 . If you would like to discuss the role before applying through the website, please contact Laura.Guascone@cromsource.com for more information.

Benefits working for TalentSource
  • Dedicated Line Manager
  • Monthly meetings with line manager
  • Employee satisfaction survey - your feedback is important for continuous improvement
  • Annual appraisals development planning
  • Yearly team event
  • New Year's diner
  • Career opportunities within both our CRO departments and our TalentSource Life Sciences Unit, locally and internationally


Why choose TalentSource Life Sciences/CROMSOURCE?

TalentSource Life Sciences is a fully dedicated flexible resourcing department at CROMSOURCE, a family owned international, full-service Contract Research Organisation. CROMSOURCE comes from the merger of MSOURCE and CROM and we have been supporting clients with outstanding clinical research and resourcing services since 1994. Successful growth has been achieved by putting high quality and client focus at the heart of everything we do and we are proud to partner with industry leading Pharmaceutical, Biotechnology, Medical Device and Marketing Communications worldwide.

Our employees are the most valuable company asset and because we want to retain our staff, we ensure they work in a friendly, family environment and develop their skills and talents. Human Resources is the fulcrum around which all activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives to all personnel clear tools to manage both internal and client processes with the same methodology. The success of these core values are evidenced by our current below industry average turnover rates.

Our approach is to equally value our clients and our own people. We know that we are not simply providing 'staff' or 'resources'. We are experts providing experts - highly talented, well trained, motivated people who make a positive difference to the work of our clients every day. Together we help our clients succeed in their work developing medicines and medical devices for patients around the world.

Keywords: Medical Writer, Medical Writing, Submissions, CRO, Outsourced, Scientific Writer, Regulatory Submissions, Regulatory Writer, Clinical Study Reports, CSRs, Permanent, Pharma, Pharmaco, Pharmaceutical, Writer

Skills: Medical Writer, Medical Writing Location: United Kingdom

Company

ClinChoice

ClinChoice is a recognized and highly respected mid-size, global, full-service contract research organization (CRO) specializing in clinical development, post-marketing, and functional service support. We provide comprehensive end-to-end solutions, taking products from early clinical development to post-approval lifecycle management. We are committed to fostering innovation in the pharmaceutical, biotechnology, medical device & diagnostics, consumer health, cosmetics, and nutraceuticals industries. Since our establishment in 1995, we have consistently delivered high-quality services and solutions throughout the entire development lifecycle of our clients’ products. We serve a wide-ranging clientele that encompasses six of the top ten pharmaceutical companies, leading medical device companies, preeminent biotechnology companies, the largest consumer health and cosmetics companies, and numerous small-to-mid-sized innovator companies. With over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific, we are positioned to fulfil our clients’ needs locally and globally.

 

We’re on a mission to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices.

 

Company info
Website
Telephone
+44 1628 566121
Location
Suite G48
268 Bath Road
Slough
Berkshire
SL1 4DX
United Kingdom

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