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Manager Clinical Research Informatics Jobs in Colorado

We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success. Job Summary: Responsible for overseeing the implementation of daily clinical study ...

We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success. Job Summary: Responsible for overseeing the implementation of daily clinical study ...

Senior Clinical Research Associate

Denver, CO · On-site +1

$110K - $138K/yr

Senior Clinical Research Associate - Oncology Phase I - Denver, CO ICON is a global healthcare ... Perform site management activities to support the client's Oncology site success and maintain a ...

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Senior Clinical Research Associate As Clinical Research Associate you will be responsible for ... Evaluates the capability of the site to successfully manage and conduct the clinical study, both ...

Be Seen First

Senior Clinical Research Associate As Clinical Research Associate you will be responsible for ... Evaluates the capability of the site to successfully manage and conduct the clinical study, both ...

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Clinical Research Psychiatrist - Denver, CO

ProTouch Staffing

Denver, CO

Other

Re-posted 1 hour ago


Job description

Part-Time Psychiatrist

 Denver, CO | ⏰ Part-Time (0-8 hours/week)


About the Role

We are seeking a Board-Certified Physician to join as a Clinical Research Physician supporting Phase I-IV clinical trials in Denver, CO . In this role, you will ensure protocol compliance, patient safety, and collaborate with sponsors, CROs, and research teams to advance multi-therapeutic studies.


Key Responsibilities
  • Serve as Principal Investigator (PI) or Sub-Investigator (Sub-I) for clinical trials.

  • Conduct medical screenings, physical exams, and assessments of study participants.

  • Provide clinical oversight and ensure adherence to study protocols, ICH-GCP, and regulatory standards.

  • Collaborate with coordinators, nurses, and research staff to maintain compliance and accurate documentation.

  • Record patient interactions, manage adverse events (AEs/SAEs), and maintain compliance with EHR/EDC systems.

  • Build and maintain strong relationships with sponsors, CROs, monitors, and IRBs.

  • Participate in site initiation visits (SIVs), monitoring visits, audits, and investigator meetings.

  • Contribute to feasibility reviews, study design, and recruitment strategies.

  • Stay current with clinical research regulations and therapeutic advances.


Qualifications
  • M.D. or D.O. with an active, unrestricted Illinois medical license.

  • Board Certification in Psychiatry.

  • Valid DEA license and BLS/ACLS certification.

  • Clinical research/clinical trials experience preferred (training available for motivated candidates).

  • Proficiency in EHR systems, medical documentation, and clinical trial platforms (EDC, CTMS).

  • Excellent communication, collaboration, and interpersonal skills.

  • Strong commitment to ethical research and patient-centered care.


Benefits
  • Flexible, part-time schedule (0-8 hours per week).

  • Opportunity to expand expertise in multi-therapeutic clinical trials.

  • Direct involvement in advancing innovative treatments through research.


Protouch Staffing logo

About Protouch Staffing

Sourced by ZipRecruiter

Protouch Staffing, based in Plano, Texas, is a leading provider in the healthcare staffing industry. Established over 30 years ago, the company prides itself on delivering quality services in the fields of nursing, allied health, pharmaceuticals, healthcare IT, and more. Committed to building lasting relationships, Protouch Staffing continually exceeds client expectations by providing unparalleled service, superior patient care, and talented healthcare professionals.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Frisco, TX, US

Year founded

1989