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

Part time/PRN position with flexible hours

To consistently embody AMR’s Core Values:

Excellence and Consistency

Collaborative Innovation

Respect for our Subjects, Sponsors and Team Members

Community

Unimpeachable Ethics

The Investigator/Sub-Investigator reports to the General Manager.

Classification: Exempt

Primary Responsibilities:

Maintain current license to practice medicine.

Assume responsibility as the Principal or Sub-Investigator for the duration of clinical trials.

Strong working knowledge of regulatory requirements and GCP standards.

Possess thorough understanding of the clinical research protocol and patient population for which the trial is designed.

Perform evaluations on subject as needed per protocol.

Complete training as required per sponsor’s vendors to obtain certification to conduct testing and rating scales for specific protocols.

Conduct testing and rating scales per sponsor’s instructions and protocols. Completion of all documentation, paper and electronic, as required per protocol.

Evaluate subjects for clinical research trials based on their past medical and psychiatric history in comparison to the protocol specific inclusion and exclusion criteria.

Evaluate subject safety and compliance with the study medication as specified in the clinical research protocol as applicable.

Provide detailed study related documentation as required by the clinical research trial to ensure data integrity.

Adhere to reporting requirements for safety reports, protocol noncompliance and any other protocol required reports.

Ensure subject’s informed consent is obtained appropriately throughout the duration of the clinical trial.

Collaborate with Site Leadership to ensure operations goals are met.

Evaluate and report all Serious Adverse Events during the trial.

Assess causality and rate severity of all AEs during the course of the protocol.

Attend Investigator Meetings and educational seminars as needed.

Desired Skills and Qualifications:

Possess a valid MD or DO medical degree, or NP license

Active license to practice medicine within state

Demonstrate leadership skills, including ability to effectively supervise individuals and teams.

Strong interpersonal and leadership skills, self-motivation, and high personal integrity and ethics required

Ability to quickly adapt to working in a wide variety of dynamic therapeutic areas of medicine.

Ability to multi-task and perform multiple critical tasks simultaneously (under dynamic and ever-changing circumstances).

Strong written, verbal communication and interpersonal skills.

Demonstrated ability to exercise standard Universal Precautions; in the alternative, the ability to quickly learn and apply Universal Precautions.

Understanding of FDA regulations, ICH guidelines and Good Clinical Practices.

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.