Scientific Specialist

Job description

A Scientific Specialist encompasses strong scientific, informational, communication and interpersonal activities, and works with a range of different departments (e.g. marketing, regulatory affairs…) within the company in order to ensure maximum information exchange and development.

Responsibilities

1. Scientific communication:

  • Act as disease expert and take lead responsibility for maintaining a comprehensive and current knowledge of a therapeutic area (collection, evaluation and managing of scientific data) and for distribution of scientific information to respective stakeholders
  • Analyse clinical trial data, prepare and report trial results at scientific meetings
  • Assist clinicians in the preparation of scientific publications and presentations
  • Provide support in formulation of publication strategies
  • Provide support in formulation of training strategies

2. Supporting marketing:

  • Provide the medical and scientific expertise in the creation of promotional materials, events (e.g. product launch) and other activities such as tender business
  • Lead literature review within a therapeutic area and translate evidence into comprehensive materials for marketing groups
  • Review marketing materials for scientific accuracy
  • Present scientific evidence at marketing events

3. Clinical development planning:

  • Support development of study designs
  • Participate in assessment of investigator initiated trial proposals so that BU can take an informed decision

4. Clinical operational activities

  • Support trial study start-up phases (support in writing study protocol, identification of investigators and KOLs, CRF review, Investigator brochure review, CA&EC assistance, support on medical and scientific questions/issues during trial follow-up phase)
  • Review CEC/DMC/Clinical trial reports

5. Regulatory activities:

  • Work with regulatory affairs and legal department to ensure that all written documents are scientifically accurate
  • Support marketing authorisation applications (reimbursement of medical devices)
  • Perform clinical evaluations

Profile
  • Medical/biomedical/scientific degree (advanced degree is a plus)
  • Experience in clinical trials and medical/scientific communication
  • Analytical mind with well-developed scientific rigor
  • Well-developed computer, communication and presentation skills
  • Team player and willing to work collaboratively across the organization, working with others to reach results/resolution
  • Strong problem solving skills
  • Travel experience
  • Experience of an international environment is a plus
  • Fluent in English and one other language
  • Ability to motivate in a dynamic environment
  • Ability to function in a self-directed manner with a high degree of independence
  • Strong personal integrity, capable to motivate others
  • Belgian residence required
Our offer
  • An attractive salary in line with your experience and skills.
  • Fringe benefits including a medical insurance, pension plan and a care plan.
  • A supporting environment.
  • Respect for the life-work balance.
  • Career planning.
  • A focus on professional and personal growth through training and coaching.
  • Room for personal engagement to help shape our company's future.
Location
Brussels
Contact person

Evelien Van Eecke

Personal profile
Attachments
PDF, DOC, DOCX (5MB)
Contact details
Evelien
Van Eecke
Recruitment Specialist

Do you want to learn more about Fern Valley? Are you interested in seeing how we can help your company grow? Let's get acquainted. I'll be delighted to hear your story and to share our vision. Experience the personal & open approach of Fern Valley and embark on a journey with us.

+32 476 98 62 94
evelien.vaneecke@fern-valley.com