Job Description
Certified Mobile Research Physician (CMRP)
The Certified Mobile Research Physician (CMRP) is being engaged by PCM Trials to conduct objective clinical research that generates independent, high quality and reproducible results on a clinical study for a pediatric population. The CMRP will perform the clinical research duties assigned to a physician in the study protocol and delegated to the CMRP by the study investigator. The CMRP is responsible for performing physical examinations on study participants and generating accurate source documentation. The CMRP is also responsible for coordinating with the necessary site and PCM Trials staff to assure research is conducted in accordance with the study protocol, applicable state and federal regulations, Good Clinical Practice, and the applicable PCM Trials’ policies and procedures.
Qualifications
* A medical degree from an accredited medical school with current GMC Registration with License to Practice and no restrictions on practice
* UK Right to Work without restriction
* Current practice with paediatrics is a mandatory requirement for this role. Further experience in neurology and/or clinical trials is advantageous.
* Current Basic Life Support (BLS)/Advanced Cardiovascular Life Support (ACLS) & Paediatric Advanced Life Support (PALS)/EPALS certifications
* Proficient with Microsoft Office Suite
* Demonstrated leadership skills, including strong communication, written and interpersonal skills
* Reliable transportation to get to/from trial participant’s location. Driving license and access to own vehicle is strongly preferred.
Essential Functions/Areas of Accountability
* Perform the full scope of physician duties designated by the study protocol and delegated to the CMRP by the study investigator, to include comprehensive physical examinations.
* Set appointments with trial participants within the required appointment window.
* Complete mobile study visits with clinical trial participants while communicating with the study investigator through a telehealth platform.
* Work cooperatively with PCM TRIALS Clinical Project Management staff and site personnel to complete visits and submit accurate source documents in a timely manner.
* Maintain all necessary current licenses, certifications, credentialing materials and other required documents.
* Immediately notify PCM Trials’ Lead Project Manager if CMRP is the subject of any action, suit, claim, investigation, legal or administrative action, or if CMRP has knowledge of any such pending or threatened action.
* Maintain the privacy of human research participants and the confidentiality of all study data. Conduct the study in strict accordance with the approved research protocol, Good Clinical Practice, the processes and procedures established by PCM Trials, the site, and the study sponsor.
* Conducts the study visits in accordance with visit training provided by PCM Trials’ Project Management team.
* Other duties as may be assigned by PCM TRIALS or the study investigator.