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Parexel · parexel.com

Associate Clinical Research Nurse (Temporary Student Contract)

47dposted dateHealthcare / Nursing

The board publishes a posting date, so the age counts from that date.

Location
Germany - Berlin
Department
not stated
Type
not stated
Seniority
junior
Salary
not published
Posted
2026-08-24 (startDate)
First seen
2026-09-27
Classified by
rules
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Job description (as published)

When our values align, there's no limit to what we can achieve.   At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Are you a driven student with a passion for clinical research and data excellence? Join Parexel's dynamic Clinical Operations team as an Associate Clinical Research Nurse and gain hands-on experience in one of the world's leading clinical research organizations. In this role, you'll support critical clinical trial operations, contribute to quality-driven processes, and work alongside experienced professionals who are committed to advancing patient care through rigorous data management and analysis. This is a great opportunity for students to gain experience in the world of clinical trials. This is a 12-month, part-time contract: 16 hours per week (+25%) This role is fully office-based in Berlin. Key Responsibilities: •    Admit and orientate study participants within the Unit and deliver study specific presentation •    Perform acquisition of ECG and blood pressure measurements •    Stick the blood containers, fill and make ready the study material, clear up on the ward, hygienic work, maintenance of medical devices •    Perform venipuncture and cannulation for blood sampling •    Prepare required devices and study participants for Holter/Telemetry monitoring as per protocol requirements •    Obtain urine and fecal collections as per protocol requirements •    Use of psychological and physiologic test procedures •    Preparation of the documents needed for the tests (copy work, enter head data in the Case Report Forms, data transfer) •    Assist in compiling appropriate responses to internal and sponsor data queries and audit observations in a timely manner •    Participation in internal meetings as required •    Undertake any tasks that your line manager/Department Head may require from you within your scope of work. Required Qualifications: Education -   Currently pursuing a nursing or medical degree or equivalent qualification Skills & Competencies -    Fluent German and good written and oral English proficiency -    Proficient with Windows Office applications -    Strong organizational and time management skills -    Ability to work effectively under pressure -    Flexibility with shift work (early, late, night shifts) -    Availability for weekend and holiday work -    Attention to detail and commitment to data accuracy -    Strong communication and teamwork skills.