Site Care Partner, Senior CRA - Sponsor Dedicated

This is a fully remote position, open to applicants in Belgium.

📋 Description

• The Site Care Partner serves as the primary liaison for investigative sites, focusing on building and nurturing site relationships while ensuring efficient operational execution with high quality.

• Facilitates processes aimed at optimizing country and site selection and leads site start-up activities through to activation.

• Confirms that the process of obtaining informed consent has been properly conducted and documented for each subject/patient as necessary.

• Exhibits a strong commitment to safeguarding the confidentiality of every subject/patient.

• Evaluates factors that may impact the safety of subjects/patients and the integrity of clinical data at an investigator/physician site, including protocol deviations/violations and pharmacovigilance concerns.

• Oversees site management from start-up through to conduct and closeout, including planning and executing site recruitment.

• Functions as the operational point of contact for site-related inquiries, coordinating and escalating issues to the appropriate team members.

• Acts as a local/country Subject Matter Expert regarding regulations and operational implementation.

• Understands the project scope, budgets, and timelines for both personal and team activities within the clinical team; manages site-level communications and activities to ensure the achievement of project objectives, deliverables, and timelines.

• Must be capable of swiftly adapting to changing priorities in order to meet goals and targets.

• Prepares for and participates in Investigator Meetings and/or in-person sponsor meetings.

• Engages in and may lead global clinical monitoring/project staff meetings (including Sponsor representation, as applicable) and attends clinical training sessions as per project-specific requirements.

• Offers guidance at both the site and project levels regarding audit readiness standards and supports preparation for audits and necessary follow-up actions.

⛳️ Requirements

• Bachelor's degree or RN in a relevant field or an equivalent combination of education, training, and experience.

• Familiarity with Good Clinical Practice/ICH Guidelines and other relevant regulatory requirements.

• Several years of CRA experience in Belgium.

• Must possess strong computer skills and be willing to adopt new technologies.

• Exceptional communication, presentation, and interpersonal skills are essential.

• A moderate level of critical thinking skills is anticipated.

• Fluency in both Dutch and French is required.

• Capability to manage necessary travel for monitoring visits.

🏝️ Benefits

• We are dedicated to developing our team members through career advancement and growth opportunities.

• Supportive and engaged line management.

• Training in technical and therapeutic areas.

• Peer recognition and a comprehensive rewards program.

• We are committed to fostering an inclusive culture where you can genuinely be yourself.