Clinical Trial Physician - Phase I (EMEA)

Thermo Fisher Scientific

Netherlands

Remote

Entry

posted 9 days ago

About Thermo Fisher Scientific

About Thermo Fisher Scientific Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD.

For more information, please visit www.thermofisher.com.

The Role

At Thermo Fisher Scientific, you'll engage in impactful work that contributes to global health. Join our mission to enable customers to create a healthier, cleaner, and safer world. We empower our teams with the resources necessary to achieve their career goals while advancing science through the development and delivery of transformative therapies. With clinical trials conducted in over 100 countries and a commitment to innovative clinical research frameworks, your efforts will enhance health outcomes for communities now and in the future.

The Role

As a Clinical Trial Physician, you will provide essential medical leadership within the study team, collaborating closely with cross-functional members to ensure the delivery of reliable, high-quality study data on time and within budget.

Responsibilities

  • Lead medical oversight for study teams, including the creation of clinical trial protocols based on the latest scientific data.
  • Contribute to site selection and review of study protocols, amendments, Clinical Study Reports (CSRs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), and protocol deviation decisions.
  • Conduct real-time medical monitoring of clinical studies, ensuring the medical validity of primary endpoints and the safety of study subjects.
  • Proactively address and escalate medical issues in consultation with the Global Medical Indication Lead.
  • Interpret clinical trial data for regulatory documents, manuscripts, and publications as needed.
  • Serve as the medical point of contact for internal and external stakeholders, including investigators, IRBs, and Health Authorities.
  • Ensure compliance with medical aspects of studies by applying relevant SOPs and GCP.
  • Collaborate with cross-functional team members to communicate medical risks, issues, and results effectively.

Requirements

  • Medical Doctor with relevant specialty education preferred (e.g., neurology, hematology, dermatology, immunology, rheumatology, internal medicine, pediatrics).
  • Some industry experience preferred.
  • Excellent English proficiency, both written and spoken, and willingness to travel.
  • Strong interpersonal skills to lead study teams and provide medical advice.
  • Proactive problem solver with negotiation skills, sensitive to cultural needs in a global organization.
  • Strong communication skills to ensure transparency in study plans and status.

What We Offer

  • A supportive working environment that promotes health and well-being.
  • Opportunities for collaboration and professional development.

Join us at Thermo Fisher Scientific and be part of a global team that values passion, innovation, and scientific excellence. Your contributions will make a real difference in delivering tomorrow's breakthroughs. Apply today!

Required skills

dermatology

immunology

neurology

rheumatology

English

English level

Fluent

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