Study Recruiter - Early Phase Clinical Resarch

Parexel International; Berlin; Hybrid; EUR 42.000 - 54.000; Vollzeit

Zusammenfassung

Parexel International in Berlin is seeking a dynamic Study Recruiter to join our Enrollment Services team. You will identify and recruit qualified study participants while coordinating all aspects of the enrollment process, ensuring timelines are met and study milestones are achieved.

The role emphasizes organization and interpersonal skills, building relationships with physicians, managing volunteer databases, and delivering recruitment metrics to leadership and clients in a regulated clinical

Qualifikationen

• Minimum 1 year of office or database administration, telesales or customer service experience.
• Education with medical, commercial or scientific background.
• Experience with clinical research processes preferred.
• Knowledge of Good Clinical Practices and regulatory requirements beneficial.

Aufgaben

• Extract and identify qualified volunteers from medical databases, building targeted subject lists.
• Maintain and update volunteer database with precision.
• Coordinate study information sessions, screenings, and appointments.
• Explain timelines, accommodation, and expense allowances to participants.
• Deliver recruitment metrics and reports to leadership and clients.
• Coordinate with physicians and medical staff throughout screening and admission.

Jobbeschreibung

We're seeking a dynamic and results-driven Study Recruiter to join our Enrollment Services team in Berlin. You'll be at the heart of clinical research, identifying and recruiting qualified study participants while coordinating every aspect of the enrollment process. This is a pivotal role where your organizational excellence and interpersonal skills directly impact the success of groundbreaking clinical trials.

Key Accountabilities:

• Extract and identify qualified volunteers from medical databases, building targeted subject lists aligned with study protocols

• Maintain and continuously update our volunteer database with precision and attention to detail

• Leverage your knowledge of interested candidates to optimize recruitment outcomes

• Develop comprehensive expertise in study designs, inclusion/exclusion criteria, and participant requirements

• Build and maintain strong relationships with physicians throughout the screening and admission process.

Study Coordination & Enrollment

• Orchestrate study information sessions, screenings, and appointments with meticulous planning

• Keep participants informed and engaged throughout their study journey, explaining timelines, accommodation, and expense allowances

• Coordinate control examination appointments in collaboration with medical staff

• Monitor timelines rigorously and deliver real-time updates to leadership

• Manage study advertisement budgets and select media channels aligned with study needs.

Quality Assurance & Compliance

• Review study protocols and volunteer information for inconsistencies and suggest improvements

• Ensure all established timelines are met and enrollment is conducted according to sponsor protocols, GCP, and EPCU SOPs

• Perform rigorous quality control and participate in pre- and post-study audits with sponsors and regulatory staff

• Support feasibility feedback to all departments regarding new and upcoming studies.

Team Leadership & Collaboration

• Coordinate with recruitment team members to maximize enrollment potential for assigned studies

• Act as a bridge between study participants and medical/administrative staff

• Provide initial training and supervision for newly hired team members

• Participate in team meetings including study kick-offs, preparation, and initiation training

• Deliver comprehensive recruitment metrics and statistical reports to leadership, Project Management, and clients.

Knowledge and Experience

Minimum 1 year office administration, database administration, telesales experience, customer service work experience or

similar

Education with medical or commercial background

Experience with clinical research processes preferred

Knowledge of Good Clinical Practices and regulatory requirements beneficial

Education

School-leaving certificate of secondary modern school or A-level required

Commercial, medical or scientific education preferred

Fluent in German required

Basic English language skills required.