Clinical Research Associate at TMC
Boxmeer, Noord-Brabant, Netherlands -
Full Time


Start Date

Immediate

Expiry Date

18 Jun, 25

Salary

0.0

Posted On

19 Mar, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Good communication skills

Industry

Pharmaceuticals

Description

Netherlands Life Sciences Boxmeer Hybrid
Passionate about advancing veterinary medicine?
About The Member Company

We are a global high-tech consultancy company with a team of entrepreneurial engineers, scientists, and digital experts from around the world. Together we form a fast-growing and proud community. We offer consultancy services to high-profile clients globally in diverse service areas, such as:

  • Technology & Engineering
  • Energy & Renewables
  • Life sciences & Pharma
  • Digital & IT
Responsibilities
  • Design and organization of clinical studies that meet scientific and regulatory requirements. This includes the setting of objectives, budgetary aspects, resources, timelines and the study protocol.
  • Prepare the Study Protocol.
  • Select the Investigators, laboratories and/or CROs for the study.
  • Ensure the timely selection and ordering of (I)VP and CP.
  • Ensure compliance of the administrative aspects of the study (budgets and agreements) with the applicable policies and procedures.
  • Plan and coordinate the monitoring and data management activities of each study.
  • Ensure that the study is conducted according to legal requirements, GCP and the applicable internal policies and procedures.
  • Prepare the Final Study Report.
  • Maintain contact with the all stakeholders (project leader, RA, Quality Assurance etc.) and keeps them informed of the study progress
Loading...