Clinical Research Job at Velocity Clinical Research | Apply Now
Looking for a clinical research job in the life science industry? Velocity Clinical Research is hiring a Clinical Research Coordinator I to conduct and manage clinical trials while ensuring high-quality data and patient care. This opportunity is ideal for candidates seeking growth in a fast-paced and innovative clinical research environment.
- Job Position: Clinical Research Coordinator I
- Job ID: 2025-3048
- Location: Germany
About the Company
Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites. At Velocity Clinical Research, the focus is on delivering innovative medical treatments to patients while ensuring clinical trials succeed efficiently. This life science job opportunity allows employees to grow while contributing to impactful healthcare advancements.
Job Description
This clinical research job involves conducting and managing clinical trials in accordance with study protocols, Good Clinical Practice (GCP), ICH Guidelines, and Velocity’s SOPs. The Clinical Research Coordinator I plays a key role in ensuring accurate data collection, patient safety, and successful execution of clinical studies.
Qualifications
This clinical research job role requires:
Education/Experience
- Bachelor’s degree with 1 year of relevant life science industry experience OR
- Associate’s degree with 2 years of relevant experience OR
- High school diploma/technical degree with 3 years of relevant experience
Required Certifications
- Phlebotomy (if required by state law)
- Intramuscular dose administration and preparation (if applicable)
Required Skills
- Knowledge of medical terminology
- Proficiency in computers and Microsoft Office tools
- Ability to work in a fast-paced environment
- Strong verbal, written, and organizational skills
- Excellent interpersonal and communication abilities
- Team player with multitasking capabilities
- Ability to follow guidelines and work independently
- Detail-oriented with strong problem-solving skills
- Adaptability to changing schedules
Key Responsibilities
This clinical research job role responsibilities include:
- Conduct and manage clinical trials following study protocols, GCP, ICH Guidelines, and SOPs
- Coordinate assigned trials including start-up, vendor management, and subject recruitment
- Schedule subjects, conduct visits, and ensure timely data entry and query resolution
- Manage and report adverse events, serious adverse events, and protocol deviations
- Implement protocol amendments and provide close-out reports
- Maintain confidentiality of patient and sponsor information
- Ensure patient safety and proper reporting procedures
- Create, collect, and submit regulatory documents to sponsors and IRBs
- Evaluate potential subjects through pre-screening (phone and in-person)
- Execute recruitment strategies and understand study timelines and endpoints
- Perform clinical duties such as drug administration, phlebotomy, ECG, and lab processing
- Communicate effectively with stakeholders including sponsors, CROs, and team members
Benefits
- Medical, dental, and vision insurance
- Paid time off and company holidays
- 401(k) retirement plan with company match
- Annual incentive program
- Career advancement opportunities within Velocity Clinical Research
