Care Access is looking to revolutionize access to clinical trials for the benefit of patients everywhere by advancing medical breakthroughs and uniting standard patient care with cutting-edge treatments and research.
Requirements
- Proficient at ICH/GCP, Good Documentation Practices (GDP), and ALCOA-C+.
- Strong computer skills with demonstrated abilities using clinical trials database, IVR systems, electronic data capture, MS word, and excel.
- Proficiency with technology used to support the clinical trial industry. CTMS systems like CRIO, clinical conductor, Clinical Ink; EDC systems like MediData, Oracle, and Inform; ePRO, eConsent and IWRS/IXRS, etc.
- Ability to understand and follow institutional SOPs
- Ability to communicate and work effectively with a diverse team of professionals
- Strong organizational, prioritization and leadership skills and capabilities with a strong attention to detail
- Excellent working knowledge of clinical trials, medicine and research terminology
Responsibilities
- Utilize Good Clinical Practices (GCP) in the process of screening, as well as enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.
- Review and assess protocol, study manuals, and the investigator drug brochure (including amendments) for clarity, logistical feasibility, safety, inconsistencies, etc.
- Assist PI, Regulatory, Start-up and the Clinical Trial Manager(s) to ensure that all training and study requirements are met prior to trial conduct.
- Maintain organized file for source documents, patient charts, CRFs, regulatory and study supplies
- Collect and evaluate concomitant medications
- Collect, process, and ship biological specimens as directed by protocol and/or laboratory manual.
- Accurately transcribe data to CRF or EDC.
Other
- Extensive travel required. Candidates must be willing to travel 75% of the time nationwide.
- Friendly, outgoing personality; maintain a positive attitude under pressure
- High level of self-motivation and energy
- Excellent professional writing and communication skills
- Ability to work independently in a fast-paced environment with minimal supervision
