Care Access · 1 day ago
Sub Investigator
Memphis, Tennessee, United States
Full-time
Hybrid
Senior Level
5+ years expCare Access is dedicated to improving health access and clinical research. The Sub Investigator will support clinical trial activities by overseeing study protocols, ensuring compliance, and managing patient interactions throughout the study.
Clinical TrialsHealth Care
No H1B
Responsibilities
Work closely with the Principal Investigator to oversee the execution of study protocols, delegating study related duties to site staff, as appropriate, and ensuring site compliance with study protocols, study-specific laboratory procedures, standards of Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), quality (QA/QC) procedures, OSHA guidelines, and other state and local regulations as applicable
Attends and participates in meetings with the director, other managers, and staff as necessary
Complies with regulatory requirements, policies, procedures, and standards of practice
Read and understand the informed consent form, protocol, and investigator's brochure
Be available to see subjects virtually or in-person as dictated by project design, answer their questions, and resolve medical issues during the study visit
Sign and ensure that the study documentation for each study visit is completed
Perform all study responsibilities in compliance with the IRB approved protocol
Review screening documentation and approves subjects for admission to study
Review admission documentation and approves subject for randomization
Provide ongoing assessment of the study subject/patient to identify Adverse Events
Ensure that serious and unexpected adverse events are reported promptly to the Pl
Review and evaluates all study data and comments to the clinical significance of any out of range results
Perform physical examinations as part of screening evaluation and active study conduct
Provide medical management of adverse events as appropriate
Qualification
Required
Nurse Practitioner or Physician Assistant with 5+ years of clinical experience
Currently licensed in good standing in one or more states listed above
Excellent working knowledge of medical and research terminology
Excellent working knowledge of federal regulations, good clinical practices (GCP)
Ability to communicate and work effectively with a diverse team of professionals
Strong organizational skills: Able to prioritize, support, and follow through on assignments
Strong verbal and written communication skills as evidenced by positive interactions with coworkers, management, clients and vendors
Work effectively and collaboratively with other team members to accomplish mutual goals
Strong computer skills with demonstrated abilities using clinical trials database, IVR systems, electronic data capture, MS word and excel
Ability to balance tasks with competing priorities
Critical thinker and problem solver
Curiosity and passion to learn, innovate, able to take thoughtful risks and get things done
Friendly, outgoing personality; maintain a positive attitude under pressure
High level of self-motivation and energy
Ability to work independently in a fast-paced environment with minimal supervision
Must have a client service mentality
Preferred
A minimum of 1 year of relevant work experience as Sub-Investigator in a Clinical Research setting
Benefits
Paid Time Off (PTO) and Company Paid Holidays
100% Employer paid medical, dental, and vision insurance plan options
Health Savings Account and Flexible Spending Accounts
Bi-weekly HSA employer contribution
Company paid Short-Term Disability and Long-Term Disability
401(k) Retirement Plan, with Company Match
Company
Care Access
Care Access helps people learn more about their health and participate in clinical research to help find new medicines and cures.
501-1000 employees
Funding
Current Stage
Late StageTotal Funding
unknownKey Investors
Biomedical Advanced Research and Development Authority (BARDA)
2024-08-26Grant
Leadership Team
Ahmad Namvargolian
CEO, Co-Founder
Recent News
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