Skill

Good Clinical Practices (GCP)

Certifications and Credentials

Good Clinical Practices is the plural/alternate phrasing of the same ICH-derived international standard governing the ethical and scientific conduct of clinical trials on human subjects. It covers informed consent, protocol adherence, monitoring, and data integrity requirements. Clinical trial coordinators, investigators, and sponsors are trained and certified in these practices to ensure regulatory compliance with agencies like the FDA and EMA.

Open roles requiring Good Clinical Practices (GCP) (1)

Sr. Manager - Clinical Trial Lead

Biogen

Full-time · $141,000 – $188,000

This role manages the operational delivery of clinical trials at a pharmaceutical company, overseeing study design, execution, budgets and cross-functional teams. It suits experienced clinical operations professionals who have managed outsourced trials and can balance scientific rigor with practical timelines and financial constraints.

Listed on Biogen’s careers site · Apply there ↗

Roles that use Good Clinical Practices (GCP)

• Clinical Trial Manager1

• Regulatory Affairs
• Informed Consent