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Sub Investigator Position Description

Position Overview

A perfect opportunity for doctors, PAs and APRNs who are looking for a change of pace from their day-to-day practice. AMR employs doctors, PAs and APRNs who are passionate about the future of medicine

Serve as a Sub-Investigator for clinical trials involving pharmaceuticals and medical procedures. The Sub Investigator is responsible for conducting clinical trials in accordance with the research protocol, Good Clinical Practices (GCPs), and federal / state regulations under the direction of the Principal Investigator. The Sub Investigator will collaborate with our study team, various medical and pharmaceutical companies, and regulatory personnel to ensure the health and welfare of study subjects under the direction of the Principal Investigator.

To consistently embody AMR’s Core Values :

• Excellence and Consistency
• Collaborative Innovation
• Respect for our Subjects, Sponsors and Team Members
• Community
• Unimpeachable Ethics

The Sub-Investigator reports to the Principal Investigator

Classification : Exempt

Primary Responsibilities :

Additional Responsibilities (Check If Applicable) :

Community Liaison

Support the work of AMR Investigators to the capacity of your scope of practice and advise sites and local organizations on necessary procedures and guidelines for studies that AMR will be considering and / or participating in. You will serve as a liaison between site staff, investigators, business development, community members, study participants, sponsors, CROs, IRBs to existing protocols in conjunction with Project Management to the degree that your expertise lends content to discussions. You will collaborate with Business Development to bring new study opportunities to local physicians and clinics. You will work to extend the efforts locally of the Recruitment Center for Excellence by your collaboration with community organizations and providers.

Collaborate with all clinical trial patient and staff activities to ensure safety and efficacy of study drugs and devices.

Provide local support to clinical trial recruitment procedures and deadlines, to ensure timely recruitment and retention of patients.

Act as a liaison between clinical trial sites and the clinical trial teams, ensuring that any discrepancies or alterations to protocol are addressed and actions are taken in a timely manner.

Participate in regular discussions with the clinical trial team, providing insight into regulations related to clinical trials as needed.

Develop and implement educational programs to ensure proper compliance with clinical trial protocols.

Collaborate with local organizations to provide resources, services, and education related to clinical trials.

Participate in internal and external meetings as needed to discuss and review issues related to clinical trial protocols.

Desired Skills and Qualifications :

Alliance of Multispecialty Research does not discriminate in employment on the basis of race, color, religion, sex (including pregnancy and gender identity), national origin, political affiliation, sexual orientation, marital status, disability, genetic information, age, retaliation, parental status, military service, or other non-merit factor.