Enable job alerts via email!
Boost your interview chances
Create a job specific, tailored resume for higher success rate.
An established industry player is seeking a Clinical Research Physician to lead and mentor clinical trials. This exciting role involves overseeing the safety of participants and collaborating with a diverse team in a fast-paced environment. With a commitment to regulatory compliance and excellence, this position offers the opportunity to influence the future of clinical research. If you have a passion for patient care and a strong background in clinical medicine, this is the perfect chance to make a significant impact in the field of biopharmaceuticals.
Company Description
M3 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.
As 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.
Requirements: