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Metric Bio
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  • Principal Investigator  

    - Onondaga County
    Principal Investigator – Neurology About the Role Metric Bio has been... Read More
    Principal Investigator – Neurology About the Role Metric Bio has been retained by a leading clinical research organization to identify an accomplished Principal Investigator (Neurology) to join one of the nation’s premier Centres of Excellence. The organization specializes in conducting Phase I–IV clinical trials across multiple therapeutic areas, with a strong emphasis on Neurology, Psychiatry, Acute Pain, and Dermatology . This position offers the opportunity to contribute to complex, early-phase studies in an established, well-resourced environment with full in-patient capability and an experienced clinical operations team. Key Responsibilities Provide overall leadership and oversight for the design, conduct, and reporting of clinical research studies in accordance with GCP , FDA , ICH , and internal SOPs. Ensure medical safety and high-quality clinical care for all research participants. Supervise, train, and support research staff, including sub-investigators and clinical operations personnel. Oversee patient recruitment, data integrity, protocol adherence, and regulatory compliance. Participate in sponsor meetings, investigator trainings, and industry conferences. Maintain professional communication with CROs, sponsors, and regulatory bodies. Review and provide feedback on study protocols and site performance. Requirements M.D. or D.O., Board Certified (preferably in Neurology) Minimum 3 years’ experience conducting neurological clinical trials as a Principal Investigator or Sub-Investigator Proven understanding of regulatory, ethical, and operational aspects of clinical research Active DEA license (or eligibility to obtain one) Excellent communication, leadership, and team management skills Additional Information Full-time, on-site position at a leading U.S. research centre Competitive compensation and comprehensive benefits package (medical, dental, vision, 401k, etc.) Opportunity to join a collaborative, growth-focused research organization recognized nationally for clinical excellence Confidential Application For a confidential discussion or to apply, please contact: Oli Oldham- oli.oldham@metric-search.com Read Less
  • Principal Investigator  

    - Kings County
    Principal Investigator – Neurology About the Role Metric Bio has been... Read More
    Principal Investigator – Neurology About the Role Metric Bio has been retained by a leading clinical research organization to identify an accomplished Principal Investigator (Neurology) to join one of the nation’s premier Centres of Excellence. The organization specializes in conducting Phase I–IV clinical trials across multiple therapeutic areas, with a strong emphasis on Neurology, Psychiatry, Acute Pain, and Dermatology . This position offers the opportunity to contribute to complex, early-phase studies in an established, well-resourced environment with full in-patient capability and an experienced clinical operations team. Key Responsibilities Provide overall leadership and oversight for the design, conduct, and reporting of clinical research studies in accordance with GCP , FDA , ICH , and internal SOPs. Ensure medical safety and high-quality clinical care for all research participants. Supervise, train, and support research staff, including sub-investigators and clinical operations personnel. Oversee patient recruitment, data integrity, protocol adherence, and regulatory compliance. Participate in sponsor meetings, investigator trainings, and industry conferences. Maintain professional communication with CROs, sponsors, and regulatory bodies. Review and provide feedback on study protocols and site performance. Requirements M.D. or D.O., Board Certified (preferably in Neurology) Minimum 3 years’ experience conducting neurological clinical trials as a Principal Investigator or Sub-Investigator Proven understanding of regulatory, ethical, and operational aspects of clinical research Active DEA license (or eligibility to obtain one) Excellent communication, leadership, and team management skills Additional Information Full-time, on-site position at a leading U.S. research centre Competitive compensation and comprehensive benefits package (medical, dental, vision, 401k, etc.) Opportunity to join a collaborative, growth-focused research organization recognized nationally for clinical excellence Confidential Application For a confidential discussion or to apply, please contact: Oli Oldham- oli.oldham@metric-search.com Read Less
  • Principal Investigator  

    Principal Investigator – Clinical Research Hours: Full-time, Monday–Fr... Read More
    Principal Investigator – Clinical Research Hours: Full-time, Monday–Friday, 8:00 AM – 2:30/4:30 PM Salary: $250,000 – $300,000 base + full benefits package Company: Metric Search, partnered with a leading Clinical Research Organisation About the Role Metric Search is proud to partner with a leading, multi-site Clinical Research Organisation operating across a network of 18 clinical research sites. We are seeking a Principal Investigator to join one of their established research centres, contributing to industry-leading clinical trials and advancing medical innovation. This is a full-time, on-site role with prior experience serving as a Principal Investigator (or extensive Sub-Investigator experience). Key Responsibilities Serve as the Principal Investigator for assigned clinical trials, ensuring all studies are conducted in accordance with ICH-GCP and regulatory requirements. Collaborate with study sponsors and CRO teams - acting as the site’s subject matter expert (SME) in your field. Provide medical oversight for study participants, including in-house or virtual patient calls during business hours. Rotate after-hours call duties with two other investigators (no after-hours phone coverage required individually). Participate in investigator meetings, sponsor calls, and industry conferences. Support site operations and patient recruitment during both high- and low-enrolment seasons. Ideal Candidate Board-certified. US Medical License. Experience as a Principal Investigator preferred; Sub-Investigator experience in Pfizer-sponsored or major pharmaceutical trials will be strongly considered. Committed to full-time site involvement (no multiple practice commitments). Passionate about clinical research and patient-centred science. Strong communicator with a collaborative, leadership-oriented approach. What’s on Offer Competitive base salary of $250,000 – $300,000 Relocation support provided Opportunity to work within a network of 18 sites Regular exposure to sponsors, industry leaders, and conferences If this sounds like your next step, please apply, or contact executive search consultant - Oli Oldham on oli.oldham@metric-search.com. Read Less
  • Principal Investigator  

    - Miami-Dade County
    Principal Investigator – Clinical Research Hours: Full-time, Monday–Fr... Read More
    Principal Investigator – Clinical Research Hours: Full-time, Monday–Friday, 8:00 AM – 2:30/4:30 PM Salary: $250,000 – $300,000 base + full benefits package Company: Metric Search, partnered with a leading Clinical Research Organisation About the Role Metric Search is proud to partner with a leading, multi-site Clinical Research Organisation operating across a network of 18 clinical research sites. We are seeking a Principal Investigator to join one of their established research centres, contributing to industry-leading clinical trials and advancing medical innovation. This is a full-time, on-site role with prior experience serving as a Principal Investigator (or extensive Sub-Investigator experience). Key Responsibilities Serve as the Principal Investigator for assigned clinical trials, ensuring all studies are conducted in accordance with ICH-GCP and regulatory requirements. Collaborate with study sponsors and CRO teams - acting as the site’s subject matter expert (SME) in your field. Provide medical oversight for study participants, including in-house or virtual patient calls during business hours. Rotate after-hours call duties with two other investigators (no after-hours phone coverage required individually). Participate in investigator meetings, sponsor calls, and industry conferences. Support site operations and patient recruitment during both high- and low-enrolment seasons. Ideal Candidate Board-certified. US Medical License. Experience as a Principal Investigator preferred; Sub-Investigator experience in Pfizer-sponsored or major pharmaceutical trials will be strongly considered. Committed to full-time site involvement (no multiple practice commitments). Passionate about clinical research and patient-centred science. Strong communicator with a collaborative, leadership-oriented approach. What’s on Offer Competitive base salary of $250,000 – $300,000 Relocation support provided Opportunity to work within a network of 18 sites Regular exposure to sponsors, industry leaders, and conferences If this sounds like your next step, please apply, or contact executive search consultant - Oli Oldham on oli.oldham@metric-search.com. Read Less
  • Principal Investigator  

    - Hillsborough County
    Principal Investigator – Clinical Research Hours: Full-time, Monday–Fr... Read More
    Principal Investigator – Clinical Research Hours: Full-time, Monday–Friday, 8:00 AM – 2:30/4:30 PM Salary: $250,000 – $300,000 base + full benefits package Company: Metric Search, partnered with a leading Clinical Research Organisation About the Role Metric Search is proud to partner with a leading, multi-site Clinical Research Organisation operating across a network of 18 clinical research sites. We are seeking a Principal Investigator to join one of their established research centres, contributing to industry-leading clinical trials and advancing medical innovation. This is a full-time, on-site role with prior experience serving as a Principal Investigator (or extensive Sub-Investigator experience). Key Responsibilities Serve as the Principal Investigator for assigned clinical trials, ensuring all studies are conducted in accordance with ICH-GCP and regulatory requirements. Collaborate with study sponsors and CRO teams - acting as the site’s subject matter expert (SME) in your field. Provide medical oversight for study participants, including in-house or virtual patient calls during business hours. Rotate after-hours call duties with two other investigators (no after-hours phone coverage required individually). Participate in investigator meetings, sponsor calls, and industry conferences. Support site operations and patient recruitment during both high- and low-enrolment seasons. Ideal Candidate Board-certified. US Medical License. Experience as a Principal Investigator preferred; Sub-Investigator experience in Pfizer-sponsored or major pharmaceutical trials will be strongly considered. Committed to full-time site involvement (no multiple practice commitments). Passionate about clinical research and patient-centred science. Strong communicator with a collaborative, leadership-oriented approach. What’s on Offer Competitive base salary of $250,000 – $300,000 Relocation support provided Opportunity to work within a network of 18 sites Regular exposure to sponsors, industry leaders, and conferences If this sounds like your next step, please apply, or contact executive search consultant - Oli Oldham on oli.oldham@metric-search.com. Read Less
  • Principal Investigator  

    - Duval County
    Principal Investigator – Clinical Research Hours: Full-time, Monday–Fr... Read More
    Principal Investigator – Clinical Research Hours: Full-time, Monday–Friday, 8:00 AM – 2:30/4:30 PM Salary: $250,000 – $300,000 base + full benefits package Company: Metric Search, partnered with a leading Clinical Research Organisation About the Role Metric Search is proud to partner with a leading, multi-site Clinical Research Organisation operating across a network of 18 clinical research sites. We are seeking a Principal Investigator to join one of their established research centres, contributing to industry-leading clinical trials and advancing medical innovation. This is a full-time, on-site role with prior experience serving as a Principal Investigator (or extensive Sub-Investigator experience). Key Responsibilities Serve as the Principal Investigator for assigned clinical trials, ensuring all studies are conducted in accordance with ICH-GCP and regulatory requirements. Collaborate with study sponsors and CRO teams - acting as the site’s subject matter expert (SME) in your field. Provide medical oversight for study participants, including in-house or virtual patient calls during business hours. Rotate after-hours call duties with two other investigators (no after-hours phone coverage required individually). Participate in investigator meetings, sponsor calls, and industry conferences. Support site operations and patient recruitment during both high- and low-enrolment seasons. Ideal Candidate Board-certified. US Medical License. Experience as a Principal Investigator preferred; Sub-Investigator experience in Pfizer-sponsored or major pharmaceutical trials will be strongly considered. Committed to full-time site involvement (no multiple practice commitments). Passionate about clinical research and patient-centred science. Strong communicator with a collaborative, leadership-oriented approach. What’s on Offer Competitive base salary of $250,000 – $300,000 Relocation support provided Opportunity to work within a network of 18 sites Regular exposure to sponsors, industry leaders, and conferences If this sounds like your next step, please apply, or contact executive search consultant - Oli Oldham on oli.oldham@metric-search.com. Read Less
  • Site Manager (Charlotte)  

    - Mecklenburg County
    Position Overview: Site Manager As the Site Manager, you will be the p... Read More
    Position Overview: Site Manager As the Site Manager, you will be the primary on-site leader overseeing the successful installation, commissioning, and qualification of advanced process systems at customer locations across North America. Collaborating closely with remote Project Managers and a global team, you will ensure smooth project execution while maintaining strict adherence to GMP standards. This role requires a hands-on approachespecially on smaller projectsalong with the ability to manage safety, quality, schedules, and budgets. Youll also play a vital role in client training and contribute to the ongoing development of the companys service capabilities. Responsibilities Coordinate with Project Managers to prepare and organize on-site work areas Lead and supervise installation, assembly, commissioning, and qualification activities Provide hands-on technical support when necessary Ensure compliance with safety regulations, GMP standards, timelines, and budgets Identify and resolve technical, scheduling, and resource challenges Serve as a communication hub between the company, clients, and leadership Manage receipt, inspection, and storage of materials and equipment Deliver on-site training and guidance to clients and team members Support continuous improvement initiatives and help build the service team Ideal Candidate Profile Were looking for a proactive, adaptable professional with a passion for technology and excellence. You thrive in fast-paced, evolving environments and excel at managing multicultural teams and projects across different time zones. Your commitment to results and your collaborative mindset make you a strong fit. Qualifications Minimum 5 years of technical field experience in mechanical, electrical, or automation roles, preferably within GMP-regulated environments At least 3 years in a supervisory or management position overseeing mechanical or process system installations in regulated industries Excellent organizational skills, calm under pressure, and effective team leadership Strong understanding of technical specifications, contractual obligations, and handling non-conformances Ability to recognize and encourage good work while providing constructive feedback Residence near the companys operational base preferred to support growth and leadership progression Read Less

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