Physician for Clinical Research - Internal Medicine at Marvel Clinical Research
Huntington Beach, CA 92647, USA -
Full Time


Start Date

Immediate

Expiry Date

13 Sep, 25

Salary

250.0

Posted On

13 Jun, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Flexible Schedule, Leadership

Industry

Pharmaceuticals

Description

POSITION OVERVIEW:

We are seeking a board-certified Internal Medicine Physician to provide medical leadership and expertise in clinical trials. The physician will be involved in studies evaluating new, cutting-edge treatments for a broad range of conditions commonly managed in internal medicine, including but not limited to cardiovascular disease, diabetes, hypertension, respiratory illnesses, infectious diseases, and other chronic or complex medical conditions.

QUALIFICATIONS:

  • Medical degree (MD or DO) with board certification in Internal Medicine. (required)
  • Valid and unrestricted medical license. (required)
  • Excellent communication, leadership, and collaboration skills.
    Job Types: Full-time, Part-time, Contract
    Pay: $100.00 - $250.00 per hour

Benefits:

  • Flexible schedule

Schedule:

  • Day shift
  • Monday to Friday

License/Certification:

  • Medical License (Required)

Location:

  • Huntington Beach, CA 92647 (Preferred)

Ability to Commute:

  • Huntington Beach, CA 92647 (Required)

Ability to Relocate:

  • Huntington Beach, CA 92647: Relocate before starting work (Required)

Work Location: In perso

Responsibilities
  • Provide medical oversight and leadership for clinical trials within the internal medicine therapeutic area.
  • Collaborate with clinical research teams to design, implement, and monitor study protocols.
  • Assess patient eligibility, safety, and clinical outcomes during trial participation.
  • Review and interpret clinical data, ensuring adherence to study protocols and regulatory standards.
  • Support preparation of clinical study reports, regulatory submissions, and presentations.
  • Ensure compliance with Good Clinical Practice (GCP), institutional policies, and regulatory requirements.
  • Participate in investigator meetings and liaise with sponsors, regulatory bodies, and other stakeholders.
Loading...