Sub Investigator

Care Access • Memphis, TN

98d

About The Position

The Sub-Investigator will be responsible for regional travel mixed with remote tele-medicine work to support our clinical research. Care Access is looking for Nurse Practitioners or Physicians Assistants to support clinical trial related activities in states throughout the USA.

Requirements

• Nurse Practitioner or Physician Assistant with 5+ years of clinical experience.
• Currently licensed in good standing in one or more states listed above.
• A minimum of 1 year of relevant work experience as Sub-Investigator (preferred) in a Clinical Research setting.
• 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.
• 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.

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.
• Attend and participate in meetings with the director, other managers, and staff as necessary.
• Comply 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 approve subjects for admission to study.
• Review admission documentation and approve 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 Principal Investigator.
• Review and evaluate all study data and comment on 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.

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.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: No Education Listed