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Parexel

Associate Clinical Research Nurse (Temporary Student Contract)

LocationGermany - Berlin
Work modeon-site
Typepart-time
SeniorityEntry
DepartmentClinical Operations
Company size10,000+ people
PostedAug 24, 2026 · 1mo ago
Verified live10h ago
At a glanceSummarised by Seekless from the posting.
Must have9
Currently pursuing a nursing or medical degree or equivalent qualification
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
Skills
Windows Office
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.
About the role
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.
More roles at Parexel
Clinical Trial Coordinator - Paris, France (Hybrid) - FSPManager, Medical Writing ServicesClinical Research PhysicianSenior Patient Recruitment Lead (UK)Regulatory Affairs Consultant - Regulatory Generalist
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