Protocol management jobs

Research Coordinator 2 - Department of Medicine, Division of Hematology & Oncology

University of Washington · Posted Jul 23, 2026

Open

Seattle, Washington, United States
On-site
Full-time · Mid
$67K–$84K per year

Research Coordinator 2 - Department of Medicine, Division of Hematology & Oncology

University of Washington · Posted Jul 23, 2026

Open

Seattle, Washington, United States
On-site
Full-time · Mid
$67K–$84K per year

Manager-Scientific Research

St. Jude Children's Research Hospital · Posted Nov 6, 2026

Open

Memphis, Tennessee, United States
Full-time · Manager
$95K–$170K per year
7+ years

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Lead and manage a new Biomedical Systems Core providing expertise, infrastructure, and operational support for biomedical sample preparation and imaging research.

Compensation

A reasonable estimate of the current salary range is $94,640 - $169,520 per year for the role of Manager-Scientific Research: Biomedical Systems Core.

Responsibilities

Build and lead the new Biomedical Systems Core
Support departmental in vivo and imaging-related research needs
Work closely with Comparative Medicine to manage a dedicated in vivo satellite space
Supervise and maintain an adjacent shared wet laboratory and tissue culture space
Build and lead a team of 2-3 specialized staff

Requirements

Bachelor’s degree in a relevant scientific discipline
Nice to have: experience managing people
Nice to have: leading projects end to end
Nice to have: mentoring teams

Skills

research operations protocol management regulatory compliance shared resource operations project management

Associate Manager / Manager, Project Services - Laboratories (Remote - West)

Lifelancer · Posted Nov 9, 2026

Open

Remote, United States
Remote
Full-time
$64K–$173K per year
3+ years

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Manage all laboratory aspects of clinical trial projects, serving as primary point of contact from award through start-up, maintenance, and closeout.

Compensation

The potential base pay range for this role, when annualized, is $64,200.00 - $173,000.00.

Responsibilities

Manage assigned clinical trial laboratory projects from award through closeout
Lead study set-up activities including protocol and budget review, start-up meetings, and implementation of project and risk management plans
Monitor timelines, deliverables, metrics, and budgets, including trend analysis, scope changes, and change orders
Serve as the single point of contact for sponsors, leading client communications, meetings, and issue triage and escalation
Drive timely, customer-focused problem solving and coordinate cross-functional resources to remove study obstacles

Requirements

Bachelor's Degree in Life Sciences and/or related field

Skills

project management clinical trial laboratory Lab Trial Management Systems (LTMS)Microsoft Office

Senior Research Coordinator

NYU Langone Health · Posted Nov 9, 2026

Open

New York, New York, United States
On-site
Full-time · Senior
$71K–$85K per year
4+ years

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The Ophthalmology Senior Clinical Research Coordinator (Sr.CRC) is an active participant and CRC team leader in the coordination of Ophthalmology related clinical research studies from research planning to conduct IRB-approved clinical trials and research studies, training CRCs and developing research and auditing policies for the Ophthalmology Department.

Compensation

The salary range for the role is $70,727.81 - $85,000.00 Annually.

Responsibilities

Demonstrates an in-depth understanding of and compliance with institutional and department policies and standard operating procedures such as relevant NYU, OSR, IRB and CTO policies, procedures and SOPs.
Supports the education and training of CRCs in these tasks.
Proficient understanding of protocol elements and requirements, supports the education and training of other clinical research team members on such elements and requirements.
Leads collaborative efforts with CRCs and CRNs to develop tracking forms for all active IRB-approved clinical trials and research studies.
Maintain tracking forms throughout the life cycle of the protocol and support an audit of tracking forms for patient safety and quality data acquisition.

Requirements

Bachelor degree in business, health administration or equivalent discipline
Nice to have: Clinical Research Coordinator (CRC) Certification
Nice to have: Basic medical terminology

Skills

Clinical Trials Research Asst/Data Management - Department of Surgery

University of Iowa · Posted Nov 7, 2026

Open

Iowa City, Iowa, United States
On-site
Contract · Associate

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The clinical trial research assistant/ data manager will apply clinical skills to administer, deliver, and evaluate research protocols, including subject recruitment, protocol management, and data collection.

Responsibilities

Perform clinical/health care research activities.
Screen, recruit, enroll and obtain informed consent for clinical research activities.
Educate patient scope of study, potential risks and benefits, possible alternative, and study requirements.
Relay information to principal investigator and verify patient eligibility.
Oversee the recruitment of subjects and scheduling of trial-related procedures.

Skills

Clinical research activities Informed consent Protocol management Data collection Regulatory documentation IRB submissions CRF development

Benefits

Clinical Project Manager - Sponsor Dedicated (FSP)

IQVIA · Posted Nov 5, 2026

Open

Buenos Aires, Argentina
2+ years

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Manage clinical trials at the local level, ensuring compliance with GCP, SOPs, and regulatory requirements, while coordinating budgets, contracts, and site recruitment.