Senior Clinical Research Associate - FSP Germany

Parexel; Deutschland; Remote; EUR 60.000 - 80.000; Vollzeit

Zusammenfassung

A leading biopharma company is seeking a Senior Clinical Research Associate to join their team. This home-based position involves local responsibility for study delivery and collaboration with local study teams. The ideal candidate has over 3 years of experience in a relevant field, preferably with strong oncology expertise. This role supports a science-driven approach to improve patient outcomes.

Qualifikationen

• Must have a minimum of 3 years of experience as a Clinical Research Associate.
• Experience in Pharma, CRO, or Biotech is ideal.
• Strong understanding of study drug handling is essential.

Aufgaben

• Provide local responsibility for study delivery at allocated sites.
• Act as the main contact with study sites to ensure proper conduct of the study.
• Prepare, initiate, monitor, and close centers in clinical studies.

Kenntnisse

Clinical Study Management

Monitoring

Data Management

Oncology Experience

Ausbildung

Bachelor’s degree in a related discipline

Jobbeschreibung

Overview

Parexel FSP is hiring Senior Clinical Research Associates to join us on a permanent full-time, home-based basis. Dedicated to a single sponsor in BioPharma, the role supports a science-driven approach to transform healthcare and improve patient outcomes. Turkey is a vital part of the sponsor's global network, hosting colleagues from every segment of the life sciences value chain.

Job Purpose

As a Senior Clinical Research Associate (CRA)/Clinical Monitor, you will have local responsibility for the delivery of the studies at allocated sites and will be an active participant in the local study team(s). You will work in close collaboration with other Monitors and the Local Study Team to ensure that quality and quantity commitments are achieved in a timely and efficient manner. You will be the main contact with the study site and will have responsibility for the proper conduct of the study.

The SCRA is responsible for the preparation, initiation, monitoring, and closure of an agreed number of centers in clinical studies according to Procedural Documents, international guidelines such as ICH and GCP as well as relevant local regulations, and that the centers deliver according to the commitment in the individual trials. A SCRA with longer tenure and experience may take on additional responsibilities, including tasks associated with the Local Study Manager.

Responsibilities

• Provide local responsibility for study delivery at allocated sites and participate in local study team activities.
• Act as the main contact with study sites and ensure proper conduct of the study.
• Prepare, initiate, monitor, and close centers in clinical studies in accordance with Procedural Documents, ICH/GCP guidelines, and local regulations.
• Collaborate with other Monitors and the Local Study Team to meet quality and timeline commitments.
• Potentially take on additional responsibilities related to Local Study Manager with increased tenure and experience.

Qualifications

• Minimum 3 years of experience as a Clinical Research Associate conducting all visits.
• Experience gained ideally in Pharma, CRO, or Biotech.
• Strong understanding of Clinical Study Management including monitoring, study drug handling, and data management.
• Bachelor’s degree in a related discipline, preferably in life science, or equivalent qualification.
• Strong oncology experience.

Apply today!

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