Profound Research · 4 weeks ago
Clinical Research Coordinator- Cardiology (Detroit, MI)
Detroit, MI
Full-time
Onsite
Entry, Mid Level
2+ years expProfound Research is a company focused on clinical innovation by partnering with community physicians to provide clinical research as a therapeutic option. The Clinical Research Coordinator will manage all clinical trial activities, ensuring compliance with laws and protocols while supporting the mission of improving patient care.
Clinical TrialsHealth CareMedical
Responsibilities
Conduct and manage all clinical trial activities in accordance with established research protocols and standards in compliance with all applicable laws, regulations, policies, and procedural requirements
Complete all relevant Profound Research required training, including but not limited to ICH-GCP certification and IATA certification in a timely manner
Mentor and train staff in the conduct of clinical trials, protocol requirements, communication and trial management skills
Lead, implement and coordinate duties for assigned clinical trials including but not limited to study start up, vendor management, subject recruitment, source document review and completion, protocol training, collection of regulatory documents, participant visits, timely data collection and documentation, management and reporting of adverse events, serious adverse events, and deviations, and monitoring visits and follow up
Ensure good documentation practices are applied by all team members when collecting, maintaining and correcting study data and required records of clinical trial activity including but not limited to source documentation, case report forms, queries, drug dispensation records, and regulatory forms
Communicate effectively and professionally with coworkers, leadership, study subjects, sponsors, CROs, and vendors
Collect and account for supplies from sponsors such as lab kits, ancillary supplies, and investigational products
Other duties as assigned
Qualification
Required
Bachelor's degree and 2 years relevant experience in the life science industry OR
Associate's degree with 4 years relevant experience in the life science industry OR
High School Graduate and/or technical degree with minimum of 6 years relevant experience in the life science industry AND 1 year Clinical Research Coordinator experience
Successful completion of GCP certification and Certified Clinical Research Coordinator (CCRC) certification within 6 months of being in the role
Experience performing clinical assessments, including but not limited to obtaining vital signs, EKGs, blood draws, processing/shipping lab specimens
Proficient ability to work independently, plan and prioritize with minimal guidance
Excellent attention to detail, organization, and communication with varied stakeholders
Ability to work as a team player with the ability to adapt to changing schedules and assignments
Company
Profound Research
Profound Research enables community physicians to offer clinical research as a therapeutic option to their patients.
51-200 employees
Funding
Current Stage
Growth StageLeadership Team
Gregory Sahagian
Chief Scientific Officer
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