Sr. Clinical Research Associate (Netherlands)

Independently performs, coordinates and oversees all aspects of the clinical site monitoring services, assessing protocol and regulatory compliance as per Alimentiv’s and sponsor’s standard processes, ICH/GCP guidelines and local regulation. Serves as the primary liaison between the sponsor/Alimentiv and investigative sites by playing a critical role in the execution of clinical study plans. Provides guidance and mentoring CRA I and II, collaborating effectively with cross-functional stakeholders in a dynamic, results-driven and high-accountability environment. Perform CRA Assessment Visits and participate in audits/inspections, when required.

MINIMUM EXPERIENCE REQUIREMENTS

4 - 6 years of related experience

PREFERRED EXPERIENCE REQUIREMENTS

7 – 9 years of related experience

MINIMUM EDUCATION REQUIREMENTS

(Honors) Bachelor’s degree

PREFERRED EDUCATION REQUIREMENTS

Master’s degree

LANGUAGE REQUIREMENTS

Fluent in written and verbal English

Or an equivalent combination of education and experience may be considered.

• Health Sciences, Life Sciences, Pharmacy or Nursing degree preferred, or Sr.CRA and/or ACRP Certification/Designation.

• Experience with Phase I–IV clinical trials is preferred.

• Thorough knowledge of ICH-GCP and local regulatory requirements.

• Proficient in using EDC systems (e.g., Medidata Rave, Oracle InForm), IRT, eTMF, CTMS, and Microsoft Office Suite.

• Ability to travel up to 40-60%, depending on project assignment and geographic location of sites.

• Strong interpersonal and problem-solving skills; able to work independently and within cross-functional teams.

• Great communication and organizational skills, detailed orientation and sense of urgency are required.

• Holder of a valid driver’s license.