The role involves managing and monitoring clinical research studies involving human subjects from inception to close-out according to budget and timelines
Job Summary
The role involves managing and monitoring clinical research studies involving human subjects from inception to close-out according to budget and timelines.
Candidates must ensure study data integrity and produce work abiding by applicable Regulatory statutes such as GCP.
Philips offers a hybrid work model allowing flexibility between office and home to support well-being and collaboration.
Matching Summary
The role involves managing and monitoring clinical research studies involving human subjects from inception to close-out according to budget and timelines.
Skills & Requirements
Must-have
Site assessment and monitoring experience
Knowledge of GCP regulations
Experience with CTMS and Medidata
Ability to manage multiple clinical studies
Strong organizational and communication skills
Nice-to-have
Customer-first attitude
Self-motivated individual
Matrix organization experience
Ability to influence business magnitude
Professional expertise in company products
Key Requirements
BS/BA in scientific or relevant discipline
Minimum of 3+ years prior clinical trial experience