Physician / Medical Director / Ohio / Permanent / MEDICAL DIRECTOR/ASSOCIATE MEDICAL DIRECTOR n[...]

Velocity Clinical Research, Inc.; Cincinnati (OH); On-site; USD 180,000 - 250,000; Full time

Job summary

An established industry player in clinical research is seeking a dedicated Physician / Medical Director to lead and oversee research services in Cincinnati, Ohio. This pivotal role involves acting as a Principal Investigator, ensuring the health and welfare of study participants while managing clinical trials in compliance with regulatory standards. The ideal candidate will collaborate closely with pharmaceutical companies and research sponsors, guiding clinical operations and ensuring the success of research initiatives. If you are passionate about advancing medical research and improving patient outcomes, this is a remarkable opportunity to make a significant impact.

Qualifications

• MD or DO with a valid medical license required.
• Experience in clinical research and patient safety.

Responsibilities

• Serve as Principal Investigator or Sub-Investigator for clinical trials.
• Ensure safety and welfare of study participants throughout the research process.
• Guide clinical operations and oversee compliance with regulatory standards.

Skills

Medical Direction

Clinical Research

Patient Recruitment

Regulatory Compliance

Protocol Review

Education

MD or DO

Medical License

Job description

Physician / Medical Director / Ohio / Permanent / MEDICAL DIRECTOR/ASSOCIATE MEDICAL DIRECTOR needed in Cincinnati, Ohio Job

Join Velocity Clinical Research, Inc. as a Physician / Medical Director / Ohio / Permanent / MEDICAL DIRECTOR/ASSOCIATE MEDICAL DIRECTOR at our Cincinnati, Ohio clinical research facility.

Job Overview

This full-time physician executive/clinician role involves providing medical direction, strategy, and oversight for research services. The physician will act as a Principal Investigator or Sub-Investigator, ensuring the health and welfare of study participants, overseeing medical procedures, and managing the conduct of studies in compliance with regulatory guidelines and best medical practices. Collaboration with pharmaceutical companies and study sponsors is essential to ensure medical continuity and study success.

Key Responsibilities

1. Serve as Principal Investigator or Sub-Investigator as assigned.
2. Support patient recruitment strategies to meet enrollment targets.
3. Protect the rights, safety, and welfare of study participants.
4. Provide medical direction and review of protocols in accordance with investigational plans and good clinical practice.
5. Assess the medical and scientific feasibility of new sponsor inquiries.
6. Participate in study initiation meetings and present protocols at IRB meetings.
7. Guide clinical operations, research staff, and sponsor managers.
8. Ensure all trials are conducted per protocol and regulatory standards.
9. Perform clinical assessments and evaluations of study participants.
10. Assist in facility operations as needed.

Qualifications

Required: [Specify necessary qualifications, e.g., MD or DO, license requirements, experience]

Preferred: [Specify preferred qualifications]

Additional Information

• Seniority Level: Director
• Employment Type: Full-time
• Job Function: Healthcare Provider

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