Offer summary

Qualifications:

Bachelor's degree in life sciences or related field., Proven experience in medical writing, preferably in a pharmaceutical or biotech setting., Strong understanding of regulatory guidelines and clinical trial processes., Excellent written and verbal communication skills..

Key responsibilities:

Develop and write clinical study protocols, reports, and other regulatory documents.

Collaborate with cross-functional teams to ensure accuracy and compliance of documents.

Review and edit documents prepared by other team members for clarity and consistency.

Participate in meetings with clients and stakeholders to discuss project requirements.

With over 30 years of experience, Alcedis combines medical expertise with ground-breaking technologies to pioneer data-driven clinical research. Our module-based service concept and flexible data capture systems adapt seamlessly to any project structure and accompany your entire research process - from Phase I to drug approval and beyond market access into real-world evidence.

Required profile