About the role
As a Clinical Research Coordinator, you will manage the daily operations of clinical trials, ensuring compliance with protocols and regulatory standards. Your responsibilities will include recruiting participants, overseeing study documentation, and collaborating with healthcare professionals to facilitate research activities.
Applicants should possess a robust background in clinical research and demonstrate excellent organizational skills. You will also monitor data collection processes and ensure the integrity of data throughout the study. If you are passionate about advancing medical research and have experience in clinical trials, we invite you to apply.
What you'll do
- Manage clinical trial operations and documentation.
- Recruit and screen study participants.
- Ensure compliance with regulatory guidelines.
- Collaborate with investigators and research teams.
What you'll need
- Bachelor's degree in Life Sciences or related field.
- 3-6 years of experience in clinical research.
- Knowledge of Good Clinical Practice (GCP) guidelines.
Skills
Good to have
Benefits
- Competitive salary with contract benefits.
- Flexible work hours.
- Professional development opportunities.
Interested in this role?
It takes about two minutes. Free to apply — NodHire never asks candidates for money.
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