Senior Clinical Trial Physician (m|f|d)

Miltenyi Biotec; Bergisch Gladbach; Vor Ort; EUR 80.000 - 120.000; Vollzeit

Zusammenfassung

A leading biotech company in Bergisch Gladbach is seeking a Senior Clinical Trial Physician to provide medical leadership and scientific expertise in clinical trials specifically in hemato-oncology. The role includes leading trial protocol design, ensuring regulatory compliance, and collaborating with cross-functional teams. Candidates should have an MD degree, preferably with a board certification in hemato-oncology, and possess skills in trial supervision and regulatory submissions. The position offers a supportive and inclusive work environment.

Leistungen

Flexible time management

Diversity and flat hierarchies

Creative contribution opportunities

Individual further training

30 days of vacation

Discounted bike leasing

Company pension plan

Disability insurance

Canteen access

Qualifikationen

• Strong medical and scientific background in hemato-oncology.
• Experience in clinical trial design, execution, and supervision.
• Proven experience with regulatory submissions and scientific publications.
• Industry experience in Pharma/Biotech in a global clinical development setting.
• Highly organized, detail-oriented, and proactive.
• Excellent communication and collaboration skills.

Aufgaben

• Lead the design and implementation of clinical trial protocols.
• Provide medical supervision of ongoing clinical trials.
• Review and analyze clinical trial data for regulatory documentation.
• Support the development of scientific publications and presentations.
• Ensure regulatory compliance in study conduct and safety.

Kenntnisse

EMR Systems

Post Residency Experience

Occupational Health Experience

Pain Management

SOAP

Primary Care Experience

Medical Management

Suturing

Workers' Compensation Law

Pharmacy Residency

Botox Experience

Epic

Ausbildung

Medical degree (MD) with valid license to practice

Board certification in hemato-oncology

Jobbeschreibung

Overview

As a Senior Clinical Trial Physician you will play a pivotal role in providing medical leadership and scientific expertise to ensure the successful planning execution and supervision of clinical trials in hemato‑oncology. You will contribute to study design regulatory submissions data review and publications while collaborating closely with cross‑functional teams to maintain the highest standards of patient safety and regulatory compliance.

As a valuable member of the Medical Science team

• You will lead the design and implementation of clinical trial protocols ensuring adherence to ICH‑GCP ethical standards and regulatory requirements.
• You will provide medical supervision of ongoing trials working closely with Clinical Operations and vendor Medical Monitors and support protocol amendments as needed.
• You will review and analyze clinical trial data contributing to Clinical Study Reports (CSRs) MAA / BLA submissions and other regulatory documentation.
• Next to this you will support the development of scientific publications and presentations serving as a medical and scientific interface to internal and external stakeholders including KOLs.
• You will ensure regulatory compliance providing medical guidance on safety adverse events and study conduct and contributing to the preparation of regulatory submission packages.
• In addition you will work closely with cross‑functional teams including Clinical Operations Regulatory Affairs Biostatistics and external partners to ensure the smooth execution of clinical programs and foster a culture of scientific excellence and accountability.

Qualifications

As a Senior Clinical Trial Physician you ideally hold a medical degree (MD) with valid license to practice; board certification in hemato‑oncology is strongly preferred.

• You bring a strong medical and scientific background in hemato‑oncology with proven experience in clinical trial design execution and supervision.
• You have experience with regulatory submissions (MAA / BLA) and scientific publications.
• You have industry experience in Pharma / Biotech ideally in a cross‑functional global clinical development setting.
• You are highly organized detail‑oriented and proactive with the ability to take ownership and make decisions in a fast‑paced environment.
• You are an excellent communicator and collaborator able to work effectively with Clinical Operations Regulatory Biostatistics KOLs and other stakeholders.
• You are committed to patient safety regulatory compliance and scientific integrity in all aspects of your work.

Additional Information

What we offer

• Working with free and self‑determined time management also mobile working
• An intercultural environment characterized by diversity and flat hierarchies
• Freedom to contribute creatively and play an active role in shaping the company
• Individual further training in our Miltenyi University as the core of the Miltenyi DNA
• 30 days of vacation discounted ticket to Germany (e)-bike leasing capital‑forming benefits company pension plan disability insurance canteen and much more.

Diversity is the bedrock of our creativity

Our mission

To innovate treatments and technologies and tackle the worlds most serious health challenges. And that’s why we connect the dots across various disciplines linking different perspectives skills and abilities.

You and your talent are welcome here in our inclusive and collaborative environment. So come as you are. Regardless of gender sexual identity age ethnicity religion or disability.

Become part of our team and focus on pushing the borders of medicine.

We look forward to your application

If you want to work in an open creative and supportive team this is the place for you. We look forward to receiving your application along with your salary expectations and availability.

Remote Work

No

Employment Type

Full‑time

Key Skills

EMR Systems,Post Residency Experience,Occupational Health Experience,Pain Management,SOAP,Primary Care Experience,Medical Management,Suturing,Workers' Compensation Law,Pharmacy Residency,Botox Experience,Epic

Experience

years

Vacancy

1