Key Skills

Job Description

Clinical Research Principal Investigator A new and exciting opportunity has now arising for a Principal Investigator to join us at an exciting period of growth. As part of our continued expansion, we are seeking an experienced Principal Investigators based in the Netherlands to work with us across a range of therapeutic areas. This is a flexible opportunity for medical specialists who are interested in contributing their clinical expertise to clinical research. The role will involve a combination of remote and on-site responsibilities, providing flexibility alongside existing clinical commitments. Key Responsibilities Act as Principal Investigator for allocated clinical trials, taking responsibility for appropriate medical oversight in accordance with applicable regulations and study protocols. Provide medical oversight of clinical trial conduct and participant safety at the allocated site. Undertake regular Principal Investigator oversight activities and attend meetings with relevant stakeholders. Oversee study-specific staff training and ensure appropriate delegation of study responsibilities. Maintain regular communication with Clinical Research Associates (CRAs), reviewing and addressing feedback relating to site performance. Participate in internal and external audits and regulatory inspections as required. Support the identification and referral of suitable participants for relevant clinical trials, where appropriate and in accordance with study requirements. Provide clinical guidance and support to Sub-Investigators and the wider research team when required. Promote compliance with Good Clinical Practice (GCP), study protocols and applicable regulatory requirements. Key Skills and Qualifications Qualified medical practitioner with recognised specialist expertise in one or more of the advertised therapeutic areas. Current registration with the relevant medical regulatory authority in the Netherlands, with appropriate specialist recognition. Commitment to participant safety, research integrity and high-quality clinical trial delivery. Previous experience in clinical research as a Principal Investigator or Sub-Investigator. Experience providing medical oversight within clinical trials and working collaboratively with clinical research teams. Why Join us? This opportunity offers specialists the chance to contribute to the development of innovative treatments through clinical research, working alongside an experienced clinical research organisation. The flexible working arrangement offers the opportunity to combine clinical expertise with involvement in clinical trials while supporting the delivery of high-quality, patient-focused research. For further information please reach out to: [email protected] OR [email protected]

Core Responsibilities

Serve as Principal Investigator for assigned clinical trials, providing medical oversight of trial conduct and participant safety while ensuring compliance with protocols, Good Clinical Practice, and applicable regulations. Oversee staff training and delegated responsibilities, communicate with Clinical Research Associates, support the research team, and participate in audits and inspections.

Requirements

Applicants must be qualified medical practitioners with recognized specialist expertise in one or more relevant therapeutic areas and current registration with the appropriate medical regulatory authority in the Netherlands. Previous experience as a Principal Investigator or Sub-Investigator, clinical trial medical oversight experience, and a commitment to participant safety and research integrity are required.