Clinical Research Assistant
About The Position
The Clinical Research Assistant supports the conduct of clinical trials by performing protocol-required procedures, coordinating study activities, and engaging directly with study participants. The role involves collecting and documenting clinical data, obtaining informed consent, managing investigational product accountability, processing biological samples, and maintaining regulatory documentation. The Clinical Research Assistant ensures compliance with study protocols, regulatory requirements, and company policies while meeting timelines and providing high-quality support to patients, investigators, and internal teams. The position may involve direct interaction with COVID-19-positive patients when required. Candidates who will need immigration or visa sponsorship at any time now or in the future are not eligible for this role; ACN does not provide visa sponsorship.
Requirements
- Proficiency in Microsoft Office and electronic data systems.
- Strong knowledge of medical terminology.
- Ability to work independently with minimal supervision.
- Excellent verbal, written, and interpersonal communication skills.
- Strong problem-solving skills and ability to adapt quickly in a dynamic environment.
- Outstanding customer service skills with internal teams and external stakeholders.
- Candidates requiring immigration or visa sponsorship at any time now or in the future are not eligible; ACN does not provide visa sponsorship.
Nice To Haves
- Bachelor’s degree in Biology or a related field, or equivalent clinical experience.
Responsibilities
- Communicate effectively and courteously with study participants.
- Collect patient medical histories and obtain informed consent.
- Dispense and manage study drug accountability per protocol.
- Perform protocol-specific procedures, including EKGs, vital signs, and phlebotomy.
- Collect, process, and ship biological samples, including blood, urine, and tissue.
- Verify the accuracy of collected clinical data and ensure timely documentation.
- Support temperature monitoring and investigational product storage.
- Interact directly with COVID-19-positive patients when required.
- Manage study startup documentation and training, and adhere to timelines.
- Ensure protocol requirements and deadlines are met consistently.
- Adhere to company policies, procedures, and compliance standards.
- Maintain patient confidentiality and regulatory compliance.
- Perform other duties as assigned.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Education Level
No Education Listed
