Medical Director

Warman O’Brien; Deutschland; Vor Ort; EUR 150.000 - 200.000; Vollzeit

Zusammenfassung

An established industry player is seeking a passionate Medical Director to enhance patient access to treatments for rare diseases. This pivotal role involves leading medical oversight for clinical trials and Expanded Access Programs, ensuring compliance with regulations and ethical standards. You will collaborate with investigators and regulatory agencies, providing expert guidance throughout the study lifecycle. If you have an MD degree and a strong background in clinical research, this opportunity allows you to make a significant impact in a growing clinical research organization. Join a team dedicated to improving patient outcomes and advancing medical science.

Qualifikationen

• 5+ years of experience in clinical research with a focus on medical monitoring.
• Strong knowledge of clinical trial design and regulatory standards.

Aufgaben

• Lead medical oversight of clinical trials and Expanded Access Programs.
• Collaborate with internal teams on study design and execution.

Kenntnisse

Clinical Research

Medical Monitoring

Communication Skills

Problem-Solving Skills

Regulatory Standards Knowledge

Ausbildung

MD Degree

Jobbeschreibung

Medical Director

Location:Europe | Travel up to 25%

Industry:CRO

Are you passionate about improving access to treatments for patients with rare and serious diseases? A growing clinical research organization is looking for an experiencedMedical Directorto lead medical oversight for clinical trials and Expanded Access Programs (EAPs).

About the Role:

As Medical Director, you’ll be the go-to medical expert on study protocols, ensuring clinical programs are conducted safely, ethically, and in line with regulations. You’ll work closely with investigators, regulatory agencies, and internal teams to provide expert guidance throughout the study lifecycle.

Key Responsibilities:

• Lead medical oversight of clinical trials and EAPs
• Guide investigators and ensure protocol compliance
• Monitor safety data, review adverse events, and support pharmacovigilance
• Participate in site selection, training, and investigator meetings
• Collaborate with internal teams on study design and execution
• Represent Medical Affairs in client discussions and proposals

What You’ll Need:

• MD degree with 5+ years in clinical research (medical monitoring preferred)
• Experience with EAP/CUP/NPP programs is a plus
• Strong knowledge of clinical trial design, safety monitoring, and regulatory standards
• Excellent communication and problem-solving skills
• Willingness to travel up to 25%

Interested? Apply now or please send your CV to [e-mail] to have a confidential, introductory call.