Clinical Research Assistant - on-site role About ClinSurge Research ClinSurge Research is a dynamic clinical research organization dedicated to advancing medical science through rigorous, patient ...
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Clinsurge Research
4 jobs near Columbus, OH
Clinical Research Assistant - on-site role About ClinSurge Research ClinSurge Research is a dynamic clinical research organization dedicated to advancing medical science through rigorous, patient ...
ClinSurge Research Reports to: COO Position Summary ClinSurge Research is a network of independent clinical research sites focused on cardiometabolic and primary care clinical research. The Regional ...
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ClinSurge Research Reports to: COO Position Summary ClinSurge Research is a network of independent clinical research sites focused on cardiometabolic and primary care clinical research. The Regional ...
... ClinSurge Research's clinical trial portfolio. This role is responsible for maintaining accurate CTMS study records, managing study invoicing and participant stipend processes, reviewing and ...
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... ClinSurge Research's clinical trial portfolio. This role is responsible for maintaining accurate CTMS study records, managing study invoicing and participant stipend processes, reviewing and ...
Clinical Research Coordinator
Nepean, ON · On-site
We are seeking a motivated and detail-oriented Clinical Research Coordinator (CRC) to manage and coordinate clinical research studies in accordance with Good Clinical Practice (GCP), institutional ...
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Clinical Research Coordinator
Nepean, ON · On-site
We are seeking a motivated and detail-oriented Clinical Research Coordinator (CRC) to manage and coordinate clinical research studies in accordance with Good Clinical Practice (GCP), institutional ...
Full-time
Posted 8 days ago
Job description
Clinical Research Assistant - on-site role
Role overview
What you'll do
What we're looking for
About ClinSurge Research
ClinSurge Research is a dynamic clinical research organization dedicated to advancing medical science through rigorous, patient-centered trials. We partner with leading sponsors, and healthcare systems to bring breakthrough therapies to the patients who need them most. Join a team that moves fast, works with purpose, and takes pride in scientific integrity.
Role overview
We are seeking a detail-oriented and motivated Clinical Research Assistant to support our growing portfolio of clinical trials. You will work closely with Principal Investigators, Study Coordinators, and sponsors to ensure smooth trial execution—from patient recruitment through data lock.
What you'll do
- Assist with patient recruitment, screening, and enrollment activities across multiple active protocols
- Collect, record, and verify source data in compliance with GCP guidelines and study protocols
- Enter and maintain accurate data in electronic data capture (EDC) systems
- Prepare, organize, and maintain regulatory binders (IRB submissions, essential documents)
- Coordinate and schedule subject visits, phlebotomy, lab work, and investigational product dispensing
- Communicate with sponsors, CROs, and IRBs regarding protocol queries and ongoing monitoring
- Assist in preparation for sponsor monitoring visits and regulatory audits
- Maintain investigational product accountability logs under PI supervision
What we're looking for
- Bachelor's degree in life sciences, public health, or a related field
- 0–2 years of experience in a clinical research or healthcare setting (internships welcome)
- Phlebotomy certification and with experience and proficiency
- Familiarity with GCP, ICH guidelines, and FDA & HC regulations is a strong plus
- Experience with EDC systems (Medidata Rave, INFORM, Veeva Vault) a plus
- Exceptional organizational skills and attention to detail
- Strong written and verbal communication skills
- Ability to manage competing priorities in a fast-paced environment
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