Clinical Development Liaison Innovative Oncology DACH
Clinical Development Liaison Innovative Oncology DACH
Employer Active
Job Alert
You will be updated with latest job alerts via email
Share
Job Alert
You will be updated with latest job alerts via email
Job Description
Who we are
Laboratoires Pierre Fabre employs more than 10 000 people in 41 countries.
The companys products can be found in all areas of the healthcare sector
from prescription and overthecounter medicines to dermocosmetics.
Your mission
Missions:
Local Intelligence:
- Stay updated on local landscape latest medical and scientific developments in the relevant therapeutic area(s). Provide insights to internal teams healthcare professionals and investigators.
- Mapping profiling of health care professionals / treatment center / health care organization / PAG. Deep and updated knowledge of medical (patient management according to disease unmet needs competitors) and patient pathway (including testing capabilities). Identify local patient journey.
KoL Management & Sponsor representation:
- Pierre Fabre Clinical Development local representative. Presence in congress scouting networking. Identification of centers of interest. Presentation of PF portfolio. Provide medical/scientific input into the development and of clinical trial including initiation and oversight of clinical studies within the respective therapeutic area.
- Clinical trial stakeholders Engagement: Build and maintain strong relationships with investigators and any other local stakeholder involved in clinical trials (ie. PAGs healthcareprofessionals) to provide scientific support gather insights and facilitate collaborative research opportunities.
Study Setup:
- Assist in identifying and selecting appropriate clinical trial sites including feasibility and preselection visits.
- Provide corporate with local insight on key elements of the study and review local documentation as needed.
- Contribute to regulatory process if relevant (e.g. obtention of documents mandatory for submission to EC)
- Involvement in liaising with the site on study start up activities (e.g. contract signature)
Clinical Trial conduct support:
- Collaborate with crossfunctional teams to support the planning and monitoring of clinicaltrials.
- Provide training support and guidanceto investigators and site staff ensuring protocol adherence patient safety and data quality.
- Participation to Site Initiation Visits and any other visit if specific need.
CrossFunctional collaboration
- Participation to Corporate Clinical Trial Team
In addition as required:
Develop relationships and scientific partnerships with opinion leaders and treatment centers with the goal of optimising patient care and developing clinical research.
Provide scientific and medical information in response to requests from healthcare professionals and gather information intended for the medical department specifically the Clinical Development division
Implement international and local regulations and company rules along the processes and procedures of Clinical Development activities as needed and in line with the guidance from Global Clinical Development
Arrange if necessary training or scientific support for medical representatives associated with the Clinical Development sites or medical community networks
Who you are
Requirements:
MD and/or PhD with clinical development experience
Indepth understanding of oncology precision medicine concepts their clinical translation and global landscape
Experienced in planning oversight and of clinical trials in oncology orexperienced in clinical trial conduct in investigator sites
Experienced in operating within matrixed global teams
Excellent and proactive communication skills
We are convinced that diversity is a source of fulfillment social balance and complementarity for our employees which is why our offers are open to all without restriction.
Employment Type
Full-Time
