What are the responsibilities and job description for the Clinical Research Physician - Principal Investigator position at M3 Wake Research, Inc.?
Company DescriptionM3 Wake Research, an M3USA Company, is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations (CROs). With close to 30 owned and managed research sites across the country, M3 Wake Research is one of the largest independent, multi-site clinical research companies in the US. M3 Wake Research continues to grow through acquisitions and uncompromising commitment to careful planning and execution in accordance with regulatory compliance.Conducting studies since 1984, M3 Wake Research owns a proprietary patient database of potential clinical trial participants across the US. As of today, our board-certified physicians have completed more than 7,000 successful clinical trials, while consistently exceeding sponsor expectations for integrity, timeliness, subject enrollment, human protection, and expeditious delivery of accurate evaluable data.Due to our continued growth, we are hiring for a Physician / Principal Investigator at Wake Research, an M3 company. This is an on-site role.Job DescriptionAs a Clinical Research Physician, you will provide clinical mentorship and leadership for clinical development and clinical trials conduct within our organization. You will operate in a wide range of aspects in clinical and pharmaceutical medicine and with patients, health authorities, colleagues, and biopharmaceutical companies. Your role will be focused on clinical trials, phase I to IV, where you will be responsible for assessing and following the safety of clinical trial participants and collaborating with the team with all aspects of clinical and scientific input and safety evaluation.Essential Duties and Responsibilities : Provide clinical expertise into the conduct of clinical trialsBuild positive relationships and networks with internal and external medical professionals and local opinion leadersWork closely with colleagues in other functions including Regulatory Affairs, Clinical Operations, and Patient EngagementLead and provide oversight to a team of researchers and clinical staff involved in the conduct of clinical trialsBe responsible for successful execution of research protocols according to FDA regulations and GCP guidelinesEvaluate study volunteers’ eligibility for clinical trialsPerform physical exams and assessments as required per research protocolsComplete all industry-required trainingAssess study patient health through interviews and physical examinationsCommunicate information to patients regarding diagnosis and treatment goalsReview all diagnostic reports and provide clinical direction to the study teamQualificationsRequirements : 10 years' post-training experience as a physicianCurrently licensed to practice medicine in the state of hire with no history of license suspension or debarmentCurrent board certification in specialty areaAdvanced knowledge of treatment and drug interactionsAbility to build rapport with patients and biopharmaceutical sponsorsStrong attention to detailStrong leadership qualitiesProvide clinical oversight to study teamClinical research experience preferred#J-18808-Ljbffr
