Clinical Development Liaison Innovative Oncology DACH

Pierre Fabre; Freiburg im Breisgau; Vor Ort; EUR 60.000 - 90.000; Vollzeit

Zusammenfassung

A leading healthcare company is seeking a Clinical Development Specialist to support oncology trials. The role involves engaging with healthcare professionals, managing clinical trial sites, and ensuring adherence to protocols. Ideal candidates will have an MD or PhD and experience in clinical research, particularly in oncology.

Qualifikationen

• MD and/or PhD with clinical development experience.
• Deep understanding of oncology and precision medicine.
• Experience in planning and conducting clinical trials.

Aufgaben

• Engage in congress scouting and networking for clinical trials.
• Assist in identifying and selecting clinical trial sites.
• Collaborate with teams to support trial planning and monitoring.

Kenntnisse

Presentation Skills

Time Management

Clinical Research

Communication Skills

GCP

Infusion Experience

Managed Care

Hospice Care

Conflict Management

Clinical Trials

Research Experience

Home Care

Ausbildung

MD or PhD

Jobbeschreibung

Laboratoires Pierre Fabre employs more than 10,000 people in 41 countries.

The company's products can be found in all areas of the healthcare sector, from prescription and over-the-counter medicines to dermocosmetics.

Your mission

Missions : Local Intelligence :

1. Stay updated on the latest medical and scientific developments in the relevant therapeutic areas. Provide insights to internal teams, healthcare professionals, and investigators.
2. Map and profile healthcare professionals, treatment centers, healthcare organizations, and PAGs. Gain deep and updated knowledge of medical and patient pathways, including testing capabilities, to identify local patient journeys.

KoL Management & Sponsor Representation :

1. Serve as Pierre Fabre's local representative for clinical development. Engage in congress scouting, networking, identify centers of interest, and present the PF portfolio. Provide medical/scientific input into clinical trial development, including initiation and oversight.
2. Build and maintain strong relationships with investigators and stakeholders involved in clinical trials, such as PAGs and healthcare professionals, to provide scientific support, gather insights, and facilitate collaborative research.

Study Setup :

1. Assist in identifying and selecting appropriate clinical trial sites, including feasibility and preselection visits.
2. Provide local insights on key study elements and review local documentation as needed.
3. Contribute to regulatory processes, such as obtaining documents for EC submission.
4. Liaise with sites on study start-up activities, e.g., contract signing.

Clinical Trial Conduct Support :

1. Collaborate with cross-functional teams to support planning and monitoring of trials.
2. Provide training and guidance to investigators and site staff to ensure protocol adherence, patient safety, and data quality.
3. Participate in Site Initiation Visits and other visits as needed.

Cross-Functional Collaboration

• Participate in the Corporate Clinical Trial Team.

Additional Responsibilities :

Develop relationships with opinion leaders and treatment centers to optimize patient care and advance clinical research. Provide scientific and medical information in response to healthcare professional requests and gather information for the Clinical Development division. Implement regulations and company rules aligned with Global Clinical Development guidance. Arrange training or scientific support for medical representatives involved with Clinical Development sites or networks.

Who you are

Requirements :

• MD and/or PhD with clinical development experience.
• Deep understanding of oncology and precision medicine concepts, their clinical translation, and the global landscape.
• Experience in planning, oversight, and conduct of clinical trials in oncology or investigator sites.
• Experience working within matrixed global teams.
• Excellent and proactive communication skills.

We believe diversity fosters fulfillment, social balance, and employee complementarity, which is why our offers are open to all without restriction.

Key Skills

Presentation Skills, Time Management, Clinical Research, Communication Skills, GCP, Infusion Experience, Managed Care, Hospice Care, Conflict Management, Clinical Trials, Research Experience, Home Care

Employment Type : Full-Time

Experience : Years

Vacancy : 1