Job Description

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 an Physician/ Principal Investigator at Wake Research, an M3 company. This is a part-time role with our Los Alamitos, CA site. Average hours worked will be 8 hours per week. Specialty: Endocrinology.

Job Description

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.

Essential Duties and Responsibilities:

• Provide clinical expertise into the conduct of clinical trials
• Build positive relationships and networks with internal and external medical professionals and local opinion leaders
• Work closely with colleagues in other functions including Regulatory Affairs, Clinical Operations, and Patient Engagement
• Lead and provide oversight to a team of researchers and clinical staff involved in the conduct of clinical trials
• Be responsible for successful execution of research protocols according to FDA regulations and GCP guidelines
• Evaluate study volunteers’ eligibility for clinical trials
• Perform physical exams and assessments as required per research protocols
• Complete all industry-required training
• Assess study patient health through interviews and physical examinations
• Communicate information to patients regarding diagnosis and treatment goals
• Review all diagnostic reports and provide clinical direction to the study team

Qualifications

Requirements:

• 10 years' post-training experience as a physician in endocrinology
• Currently licensed to practice medicine in the state of hire with no history of license suspension or debarment
• Advanced knowledge of treatment and drug interactions
• Ability to build rapport with patients and biopharmaceutical sponsors
• Strong attention to detail
• Strong leadership qualities
• Provide clinical oversight to the study team
• Clinical research experience

Compensation

Compensation for this role is $120-$145/hour.

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