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Freelance Consultant – SOP Update / Real-World Evidence (RWE) (M/F/D)
Tasks:
Participate in the project kick-off meeting and receive a detailed briefing on the project.
Conduct interviews and/or workshops with relevant internal stakeholders and departments to understand process requirements and expectations.
Review the current SOP and identify areas requiring revision.
Draft the updated SOP based on stakeholder feedback and align internally on the proposed process and wording.
Support the finalization of the SOP, ensuring consistency, clarity, and accurate documentation of the new process.
Prepare a training slide deck based on the updated SOP.
Qualification:
Proven experience in medical writing, particularly in the development or revision of SOPs.
Solid knowledge and understanding of Real-World Evidence (RWE) and/or Non-Interventional Study (NIS) processes.
Relevant experience within Medical Affairs, ideally in a pharmaceutical, biotech, or healthcare environment.
Strong stakeholder management and interviewing/workshop facilitation skills.
Excellent written and spoken English and the ability to translate complex processes into clear, structured documentation.
Requirements:
Start: asap
Duration: 4 months
Capacity: approx. 4–5 hours per week
Location: 100% remote
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