Clinical Research Investigator - Clinical Research (MD or DO) - Phoenix, AZ at The IMA Group
Phoenix, AZ 85012, USA -
Full Time


Start Date

Immediate

Expiry Date

18 Sep, 25

Salary

0.0

Posted On

19 Jun, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Clinical Trials

Industry

Pharmaceuticals

Description

COMPANY OVERVIEW:

The Clinical Research Division at The IMA Group is a dynamic hub of expertise and innovation, dedicated to advancing healthcare through clinical trials and studies. Our team of seasoned professionals collaborates with industry leaders, conducting patient-centric research across diverse therapeutic areas. Committed to ethical practices and regulatory compliance, we aim to pioneer groundbreaking medical solutions that shape the future of healthcare.

JOB SUMMARY:

Are you a board-certified MD or DO with a background in psychiatry or neurology, and a passion for advancing medical science? IMA Clinical Research is seeking a dedicated and detail-oriented Clinical Research Investigator to join our dynamic team at our Phoenix, AZ location.
You’ll serve as a Principal Investigator (PI) on pharmaceutical industry-sponsored clinical trials, playing a key part in groundbreaking research that impacts lives.

WHAT WE OFFER:

  • Flexible scheduling – ideal for professionals seeking part-time, full-time, or 1099 contract opportunities
  • A collaborative and supportive research environment
  • The chance to contribute to cutting-edge studies in mental health, neurology, and beyond

QUALIFICATIONS:

  • MD or DO degree
  • Active medical license
  • Prior experience as a Principal Investigator in pharmaceutical clinical trials
  • Preferably possess diversity and bilingual capabilities
  • Board certification in internal medicine

How To Apply:

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Responsibilities
  • Oversee staff and delegate duties accordingly.
  • Provide required documentation to Sponsor and IRB.
  • Maintain licenses for PI/Sub-I roles.
  • Conduct and supervise on-site investigations to ensure thorough and accurate assessments.
  • Screen potential subjects based on study criteria.
  • Ensure thorough documentation compliance.
  • Assess and report safety data and protocol issues.
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