Principal Data Manager

Posted 15 Days Ago
Be an Early Applicant
3 Locations
In-Office
Senior level
Healthtech • Professional Services
The Role
Principal Data Manager talent community candidate responsible for clinical data management across late-phase, observational, and interventional studies. The role requires oversight of vendors and stakeholders, ensuring data quality, regulatory compliance, and process improvement. Candidates should have experience in CRO, biotech, or pharmaceutical environments, knowledge of CDISC, GCP, ICH guidelines, and regulatory requirements, and proficiency with EDC systems such as Medidata Rave or Inform.
Summary Generated by Built In


Join Our Talent Community

We're not advertising a specific role today - we're proactively connecting with experienced professionals for upcoming opportunities. As part of our team, you would be working alongside passionate and innovative professionals to ensure our customers achieve their goals. By joining our talent community, you'll be among the first considered when the right role opens.

Who We're Looking to Connect With
  • Experienced Data Managers with a background in clinical research and drug development

  • Principal, Lead, or Senior Data Managers seeking their next challenge

  • Professionals with expertise in late phase, observational, or interventional studies

  • Data Management experts experienced in vendor oversight and cross functional collaboration

  • Professionals passionate about data quality, compliance, and process improvement

  • Individuals who thrive in global, remote, and highly collaborative environments

Typical Qualifications
  • Bachelor's degree in Life Sciences, Computer Science, Statistics, or a related field

  • Several years of clinical Data Management experience within CRO, biotech, or pharmaceutical environments

  • Strong knowledge of CDISC standards, GCP, ICH guidelines, and regulatory requirements

  • Experience with EDC systems such as Medidata Rave, Inform, or similar platforms

  • Proven ability to manage external vendors and multiple stakeholders

  • Excellent communication, organizational, and problem solving skills

What You Can Expect From Us

  • A review of your profile by our Talent Acquisition team

  • Direct outreach when a relevant opportunity opens that matches your experience

  • A genuine career conversation, not a transactional one

When Will You Hear From Us?

Because this is a proactive talent pool rather than a live vacancy, our response timelines work a little differently. You'll receive an automated confirmation once your details reach our system. A member of our Talent Acquisition team will then be in touch directly when a suitable opportunity arises, this could be in a few weeks, a few months, or longer depending on business needs.

We appreciate your patience and interest in TFS, your details are valued, and we'll be in touch when the timing is right.

What We Offer

We provide a competitive compensation package, comprehensive benefits, and the opportunity for personal and professional growth in a rewarding environment. You'll be joining a team that values collaboration, innovation, and making a difference in the lives of patients.

A Bit More About Us

Our journey began over 30 years ago in Sweden, in the city of Lund. As a global CRO with the ultimate goal of ensuring patients' safety and well-being, we provide biotechnology and pharmaceutical companies with tailored clinical development solutions. We currently operate in 17 countries across Europe, North America, Asia Pacific and the Middle East.

Our core values of Trust, Quality, Flexibility and Passion are what make TFS HealthScience the successful company it is today. Our values shape our culture and work ethic. They reflect what we stand for and guide our organization.

Ready to introduce yourself? Submit your CV below — there's no specific role attached. We'll be in touch when the right opportunity emerges.

#Together we make a difference

Skills Required

  • Bachelor's degree in Life Sciences, Computer Science, Statistics, or a related field
  • Several years of clinical data management experience in a CRO, biotech, or pharmaceutical environment
  • Strong knowledge of CDISC standards, GCP, ICH guidelines, and regulatory requirements
  • Experience with EDC systems such as Medidata Rave, Inform, or similar platforms
  • Experience managing external vendors and multiple stakeholders
  • Experience with late-phase, observational, or interventional studies
  • Excellent communication, organizational, and problem-solving skills
Am I A Good Fit?
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The Company
700 Employees
Year Founded: 1996

What We Do

TFS HealthScience is a global, mid-sized contract research organization (CRO) founded in Sweden. It partners with biotechnology and pharmaceutical companies across the full clinical development lifecycle, providing full-service clinical development, project-based support, strategic resourcing, and Functional Service Provider (FSP) solutions. With teams and strategic partners spanning more than 50 countries, TFS supports specialized therapeutic programs and works to advance treatments and improve patient outcomes.

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