Clinical Research Job in Germany at Velocity
Looking for a rewarding Clinical Research Job in Europe? This Clinical Research Coordinator position at Velocity Clinical Research offers a dynamic job in Germany within a fast-growing research site network. It is an excellent job opportunity for life science graduates seeking hands-on clinical trial experience, career advancement, and global exposure in clinical operations.
About Velocity Clinical Research
Velocity Clinical Research is a fully integrated research site organization dedicated to accelerating clinical trials through high-quality data and exceptional patient care. The company partners with sponsors and CROs worldwide to deliver efficient and compliant research services. Velocity invests in employee growth and supports career advancement, making it a preferred employer for professionals seeking a long-term Clinical Research Job in global markets, including Germany.
Clinical Research Job Details:
- Job Title: Clinical Research Coordinator I
- Category: Clinical Operations
- Position Type: Regular, Full-Time
- Telecommute: No
- ID: 2026-3364
Job Overview
Velocity Clinical Research is an owned and integrated research site organization dedicated to delivering excellence in patient care, high-quality data, and fully integrated research services. The organization is committed to advancing innovative medical treatments by generating high-quality clinical data efficiently while maintaining exemplary patient care standards.
Velocity fosters a performance-driven culture and supports career advancement for employees who demonstrate strong performance. The organization welcomes both individuals new to clinical research and experienced industry professionals.
Employee benefits include medical, dental, and vision insurance; paid time off and company holidays; a 401(k) retirement plan with company match; and an annual incentive program.
Clinical Research Job Summary
The Clinical Research Coordinator I conducts and manages clinical trials in accordance with study protocols, Good Clinical Practice (GCP), International Council for Harmonisation (ICH) guidelines, and Velocity’s Standard Operating Procedures (SOPs). The role supports study execution from start-up through close-out while ensuring patient safety, regulatory compliance, and data integrity.
Key Responsibilities
- Conduct and manage clinical trials in accordance with study protocols, GCP, ICH guidelines, and Velocity SOPs
- Coordinate assigned trials under supervision, including start-up activities, vendor management, subject recruitment, source documentation review, scheduling, protocol training, regulatory document collection, and study visits
- Ensure timely data entry and resolution of queries in sponsor data systems
- Manage and report adverse events (AEs), serious adverse events (SAEs), and protocol deviations
- Implement protocol amendments and prepare close-out reports
- Develop and implement research and administrative strategies to manage assigned protocols
- Communicate professionally with coworkers, leadership, study subjects, sponsors, CROs, and vendors
- Apply Good Documentation Practices (GDP) in data collection, correction, transfer, and query resolution
- Maintain confidentiality of patient protected health information and sponsor/company confidential information
- Uphold patient safety standards and ensure proper reporting of all safety events
- Ensure staff delegation, training, and documentation compliance
- Create, collect, and submit regulatory documents to sponsors and IRBs per protocol and regulatory requirements
- Evaluate potential study participants through phone and in-person pre-screens
- Execute recruitment strategies defined by the Clinical Research Team
- Maintain understanding of protocol timelines, endpoints, vendors, and target patient populations
- Perform clinical duties within scope of practice (e.g., drug preparation and administration, FibroScan, phlebotomy, ECG, laboratory processing)
- Promote respect for cultural diversity and professional conduct at all times
Education & Experience Requirements
- Bachelor’s degree with 1 year of relevant life science industry experience, or
- Associate’s degree with 2 years of relevant life science industry experience, or
- High school diploma and/or technical degree with a minimum of 3 years of relevant life science industry experience
Required Licenses/Certifications
- Phlebotomy certification (if required by state law)
- Intramuscular dose administration and preparation certification (if required by state law)
Required Skills
- Knowledge of medical terminology
- Proficiency with computers and Microsoft Office software
- Ability to operate office equipment (fax, copier, multi-line telephone)
- Ability to work in a fast-paced environment
- Strong verbal, written, organizational, and interpersonal communication skills
- Ability to work effectively as part of a team
- Ability to read, write, and speak English
- Ability to multitask and follow written guidelines
- Ability to work independently, plan, and prioritize with limited supervision
- Flexibility and adaptability in response to rapidly changing schedules
- Strong attention to detail
- Problem-solving and strategic decision-making skills
- Professionalism and accountability for individual responsibilities
Physical Requirements
- Ability to sit or stand for extended periods
- Ability to travel locally and nationally
- Ability to communicate in person and via telephone
- Limited walking required
- Ability to lift up to 30 pounds
