Enable job alerts via email!

Senior Clinical Data Manager* (located in United Kingdom)

Metronomia Clinical Research GmbH

London

Hybrid

GBP 125,000 - 150,000

30+ days ago

Boost your interview chances

Create a job specific, tailored resume for higher success rate.

Job summary

Join a forward-thinking company as a Senior Clinical Data Manager, where you will lead projects and ensure excellence in clinical data management. You'll play a vital role in managing clinical studies, collaborating with teams, and representing the company in key interactions. Enjoy a supportive environment that values your contributions and offers hybrid working models, competitive remuneration, and opportunities for professional growth. If you are passionate about clinical research and want to make a difference in a dynamic team, this role is perfect for you.

Benefits

Hybrid working models

Attractive remuneration

Extensive company social benefits

Internal and external training opportunities

Flat hierarchy

Qualifications

  • At least 3 years of experience in Clinical Data Management in the pharmaceutical industry.
  • Sound knowledge of GxP-regulated clinical research and CDISC standards.

Responsibilities

  • Lead study projects in Clinical Data Management and coordinate project teams.
  • Involved in eCRF/ePRO setup, data review, and cleaning.

Skills

Clinical Data Management

GxP regulations

CDISC standards

Communication Skills

Team Collaboration

Education

Relevant degree or training

Tools

eCRF/ePRO systems

Job description

Since 1990, METRONOMIA has stood for quality, competence, continuity and unconditional customer orientation in terms of data management, statistical services and medical writing in clinical research. As a growth-oriented medium-sized company with over 140 employees, we operate internationally. Our customers appreciate the competence and commitment of our employees and we value our employees as the basis of the company's success. Join a motivated and friendly team as

Senior Clinical Data Manager (m/f/d)
Your responsibilities
  • You will lead study projects in the area of Clinical Data Management or represent and coordinate Metronomia project teams as project manager.
  • You represent Metronomia in project meetings with customers and study teams and, if desired, in other customer interactions (e.g. bid defense meetings).
  • You are actively involved in the clinical data management of clinical and non-interventional studies. This includes tasks in eCRF/ePRO setup and validation, DMP development, data review & cleaning and import of external data.
  • You actively support the further development of the Clinical Data Management SOPs.
  • You have relevant training or a degree and at least 3 years of professional experience in Clinical Data Management in the pharmaceutical industry or a CRO.
  • You have a sound knowledge of GxP-regulated clinical research, clinical data management processes and CDISC standards.
  • You are a team player with high social competence and very good communication skills.
  • You communicate confidently both verbally and in writing.
Our offer for you
  • Appreciation and family-friendliness! We see and respect you as a person and support your professional compatibility with hybrid working models.
  • Excellence is worth it! We offer attractive remuneration and extensive company social benefits!
  • Flat hierarchy! Our entire team meets at eye level at all times! In this way, we create a special working atmosphere for our highly motivated and qualified team!
  • Challenging tasks! There is a detailed introduction to the area of responsibility and regular opportunities for internal and external training!
Have we piqued your interest? We look forward to getting to know you!

Please send us your CV or your LinkedIn profile including details of your possible start date and salary expectations. If you have any questions about the position and the application process, please do not hesitate to contact our HR Manager Christoph Hortian (+49 - 89 - 829 265 101 / chortian@metronomia.net) .

Get your free, confidential resume review.
or drag and drop a PDF, DOC, DOCX, ODT, or PAGES file up to 5MB.