Medical Affairs Director
Location: BelgiumSIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!
THE COMPANY
Our client is a professional Biotechnology organization, based in Waals-Brabant Belgium.
They are pioneers in developing therapies for patient with life threatening diseases. They are dedicated to innovation in clinical trials, as well as a strong expertise in cell manufacturing.
ROLE DESCRIPTION
In this role you will be responsible for providing medical guidance and direction throughout the development and conduct of clinical trials in the oncology area.
RESPONSIBILITIES
- Ensure keeping up to date with technical and scientific developments and provide medical and scientific support to the research teams and departments
- Identify significant developments in the field, and establish ongoing liaisons with key opinion leaders, government officials, healthcare organizations and medical professionals
- Act as medical resource to the company's Clinical Research for protocol design, CRF content, adverse events, discussions and guidance towards investigators
- Play an active role in business development by translating client needs
- Participate in project bids and client presentations
- Provide support and information to other departments. In stage of new clients, support other departments with evaluating the project feasibility, and discussion of project details in face-to-face meetings with clients
- Provide support towards sponsors for the development of early phase clinical trial programs
REQUIREMENTS
- Medical qualification (MD) with specialty training in oncology preferred
- Working experience in immunology-oncology is highly desirable
- At least 3 to 5 years clinical experience in biopharmaceutical, biotechnology industry
- Knowledge of clinical stage drug development efforts
- Experience preparing and reviewing documents for clinical development to ensure highquality
document submissions health authorities and regulators
- Experience of cross-functional team with diverse skill sets
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Laura Hoekstra.
