We are seeking a motivated Junior Real-World Evidence (RWE) Expert to join our team within the rheumatology department. This position is vital for ensuring that ongoing studies are delivered on time and meet the highest quality standards. The candidate will work closely with cross-functional teams, including medical, market access, and safety, to support the design and delivery of RWE studies. The role will initially focus on tracking deliverables, quality assurance, and supporting the publication process. By Q4, there will be an opportunity to take on more responsibilities related to the initiation of new protocols under supervision.
Key Responsibilities:
• Monitor ongoing RWE projects and ensure deliverables are met on time with the required quality.
• Familiarize with the project objectives and study designs to ensure alignment with company needs.
• Collaborate with vendors and internal teams to ensure the studies are conducted correctly and according to protocol.
• Support the initiation of new studies and protocols under supervision, particularly towards the end of the year.
• Participate in publications related to the studies and ensure accuracy and compliance.
• Communicate effectively with cross-functional teams (e.g., medical, market access, safety).
• Maintain a strong understanding of RWE principles, including pharmacology and epidemiology.
Must-Have Qualifications:
• Experience: 1 to 3 years in Real-World Evidence (RWE), pharmacology, pharmacoepidemiology, or related fields.
• Educational Background: Degree in pharmacology, epidemiology, statistics, or related field.
Skills:
• Strong communication skills, attention to detail, and the ability to work independently and in a team.
• Language: Fluent in English (communication with international teams and vendors).
• Agility and Learning Mindset: Open to learning and exposure to different aspects of the field.
Nice-to-Have Qualifications:
• A proactive mindset with the ability to manage multiple tasks.
• Strong communication skills and the ability to work in a collaborative environment.
• Eagerness to learn and take on new challenges.
• A solid understanding of the theoretical aspects of RWE, including pharmacoepidemiology or related studies.
• Background or experience in different therapeutic areas, which demonstrates adaptability.
• Experience in working with both CROs and pharmaceutical companies.
• Strong interpersonal skills, ability to work in a collaborative environment, and agile in decision-making.
• Any additional languages would be a plus, but not a requirement.
Workplace & Conditions:
• Location: The position is open for 100% remote work, though candidates are welcome to meet the team occasionally at the Brussels headquarters. Regular visits are not required but may be beneficial.
• Contract Type: Full-time