We have other current jobs related to this field that you can find below

  • Clinical Trial Specialist

    1 month ago

    Jersey City, New Jersey, United States Actalent Full time

    Job Title: Clinical Trial Specialist Job Description The Clinical Trial Specialist coordinates the initiation and activation of all new clinical trial protocols ensuring compliance with Scientific Review Board (SRB), Institutional Review Board (IRB), Human Research Oversight Committee (HROC), data collection plans, and finance/contract approvals. This role...

  • Clinical Trials Nursing Specialist

    6 days ago

    Neptune City, New Jersey, United States Hackensack Meridian Health Full time

    Position OverviewClinical Research NurseAt Hackensack Meridian Health, our mission is to enhance the lives of our patients through exceptional care. As a Clinical Research Nurse, you will play a vital role in this mission by ensuring the integrity and compliance of clinical trials.Key ResponsibilitiesEnsure timely submission of all protocol amendments,...

  • Senior Clinical Trial Management Specialist

    7 days ago

    Foster City, California, United States Integrated Resources, Inc Full time

    Job OverviewPosition Title: Senior Clinical Trial Management SpecialistLocation: RemoteContract Duration: 06+ monthsCompensation: $60 - $64/hr. on W2Position Summary:As a Senior Clinical Trial Management Specialist, you will play a pivotal role in the execution of clinical trials across various phases, ensuring adherence to established protocols and...

  • Senior Clinical Trial Management Specialist

    6 days ago

    Foster City, California, United States LeadStack Inc. Full time

    Position Title: Senior Clinical Trial Management SpecialistDuration: 6 months with potential for extensionLocation: RemoteCompensation: $40-$55/hr on W2Department: Clinical Operations – Biomarker and Bioanalytical OperationsClinical Operations is tasked with the global execution of all Phase I - IV clinical trials across various therapeutic areas. This...

  • Lead Clinical Researcher

    1 day ago

    Jersey City, New Jersey, United States DM Clinical Research Full time

    Job OverviewLead Clinical Researcher (MD/DO)The Lead Clinical Researcher will oversee all clinical trials in alignment with ICH, GCP, local regulations, study protocols, and organizational procedures.Key ResponsibilitiesGuarantees the medical safety and well-being of study participants through the diligent execution of clinical trials.Supports the...

  • Lead Clinical Research Investigator

    1 day ago

    Jersey City, New Jersey, United States DM Clinical Research Full time

    Job OverviewPosition: Principal Investigator (MD/DO)The Principal Investigator will oversee all clinical trials in accordance with ICH, GCP, local regulations, study protocols, and organizational procedures.Key ResponsibilitiesSafeguards the medical well-being and safety of study participants through the diligent execution of clinical trials.Maintains...

  • Clinical Trials Management Specialist

    6 days ago

    Foster City, California, United States Rose International Full time

    Minimum Education & Experience: MA/ MS / PharmD / PhD with a minimum of 2 years of relevant clinical or related experience in life sciences. BA / BS / RN with at least 4 years of relevant clinical or related experience in life sciences. Proven experience in overseeing the work of external vendors. Fulfillment of all criteria for the Clinical Trial Management...

  • Clinical Trials Operations Specialist

    6 days ago

    Foster City, California, United States Rose International Full time

    Minimum Education & Experience: MA/ MS / PharmD / PhD with a minimum of 2 years of relevant clinical or related experience in life sciences. BA / BS / RN with at least 4 years of relevant clinical or related experience in life sciences. Proven experience in overseeing the activities of external vendors. Must fulfill all qualifications for the Clinical Trial...

  • Clinical Trials Operations Specialist

    7 days ago

    Foster City, California, United States Rose International Full time

    Minimum Education & Experience: MA/MS/PharmD/PhD with a minimum of 2 years of relevant clinical or related experience in life sciences. BA/BS/RN with at least 4 years of relevant clinical or related experience in life sciences. Proven experience in overseeing the work of external vendors. Must meet all qualifications for the Clinical Trial Management...

  • Clinical Trials Operations Specialist

    6 days ago

    Foster City, California, United States Rose International Full time

    Minimum Education & Experience:MA/MS/PharmD/PhD with over 2 years of relevant clinical or related experience in life sciences.BA/BS/RN with 4+ years of relevant clinical or related experience in life sciences.Proven experience in overseeing the work of external vendors.Meets all qualifications for Clinical Trial Management Associate (CTMA) grade 25 position...

  • Clinical Trials Nursing Specialist

    6 days ago

    Neptune City, New Jersey, United States Hackensack Meridian Health Full time

    Position OverviewClinical Research NurseAt Hackensack Meridian Health, our dedicated teams strive to enhance the lives of our patients by delivering exceptional care every day. Our extensive range of services enables you to utilize your expertise across various environments while advancing your career within New Jersey's leading healthcare system.Key...

  • Clinical Trial Manager

    2 days ago

    daly city, United States PinkDx, Inc. Full time

    Job Title: Clinical Trial Manager Location: San Francisco Bay Area Job Type: Full-TimeAbout Us:PinkDx is an early-stage company focused on positively impacting the health of women throughout their life journey. Our vision is to identify unmet medical needs that are unique to women, address them with scientific rigor, and provide answers that have an...

  • Clinical Trial Manager

    4 weeks ago

    Daly City, United States PinkDx, Inc. Full time

    Job Title: Clinical Trial Manager Location: San Francisco Bay Area Job Type: Full-TimeAbout Us:PinkDx is an early-stage company focused on positively impacting the health of women throughout their life journey. Our vision is to identify unmet medical needs that are unique to women, address them with scientific rigor, and provide answers that have an...

  • Clinical Trial Manager

    4 weeks ago

    Daly City, United States PinkDx, Inc. Full time

    Job Title: Clinical Trial Manager Location: San Francisco Bay Area Job Type: Full-TimeAbout Us:PinkDx is an early-stage company focused on positively impacting the health of women throughout their life journey. Our vision is to identify unmet medical needs that are unique to women, address them with scientific rigor, and provide answers that have an...

  • Unblinded Clinical Research Coordinator I

    1 month ago

    Jersey City, United States DM Clinical Research Full time

    Job DescriptionJob DescriptionUnblinded Clinical Research Coordinator IDM Clinical Research is looking to hire an Unblinded Clinical Research Coordinator to join our team. This individual will be responsible for dispensing Investigational Products (IP) as part of clinical research trials.Duties & Responsibilities:Compound and dispense prescribed IP.    ...

  • Clinical Trials Manager

    2 months ago

    Oklahoma City, Oklahoma, United States University of Oklahoma Full time

    OU Health Stephenson Cancer Center is Oklahoma's only National Cancer Institute (NCI)-Designated Cancer Center, and one of only 72 NCI-Designated Cancer Centers in the United States. This highly competitive accreditation ensures that our patients receive the highest standard of care and have access to the most advanced cancer treatment options. At the...

  • Lead Clinical Researcher

    1 day ago

    Jersey City, New Jersey, United States DM Clinical Research Full time

    Job OverviewLead Clinical Researcher (MD/DO)The Lead Clinical Researcher will oversee all clinical trials in accordance with ICH, GCP, local regulations, study protocols, and organizational procedures.Key ResponsibilitiesGuarantees the medical welfare and safety of participants through the careful execution and management of studies.Assists in ensuring...

  • Clinical Research Coordinator III

    2 months ago

    Jersey City, United States DM Clinical Research Full time

    Job DescriptionJob DescriptionClinical Research Coordinator IIIA CRC III will ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. To ensure study enrollment meets or exceeds Sponsors' expectations. To...

  • Clinical Research Coordinator III

    3 days ago

    Jersey City, United States DM Clinical Research Full time

    Job DescriptionJob DescriptionClinical Research Coordinator IIIA CRC III will ensure that quality research is conducted at assigned investigative sites in accordance with the sponsor protocol, FDA Regulations, and ICH/GCP guidelines and to provide the best quality data to the sponsor. To ensure study enrollment meets or exceeds Sponsors' expectations. To...

  • Clinical Trials Coordinator

    1 day ago

    Kansas City, Missouri, United States Medix™ Full time

    Job Title: Clinical Trials CoordinatorWelcome to Medix™, where we are seeking a committed Clinical Trials Coordinator to enhance our research initiatives.Overview:In this position, you will be responsible for ensuring that approved research protocols are effectively executed and adhered to. You will facilitate the informed consent process, oversee patient...

Clinical Trial Specialist

1 month ago

Jersey City, United States Actalent Full time

Job Title: Clinical Trial Specialist

Job Description

The Clinical Trial Specialist coordinates the initiation and activation of all new clinical trial protocols ensuring compliance with Scientific Review Board (SRB), Institutional Review Board (IRB), Human Research Oversight Committee (HROC), data collection plans, and finance/contract approvals. This role involves preparing study tools, developing study tools using Oncore/Excel/Word, reviewing patient charts to confirm protocol eligibility, and maintaining research records. Additionally, the specialist will register consented research patients with study sponsors, assist in grading adverse events, serve as a liaison with study sponsors, and ensure that all personnel are conducting the study according to the treatment plan and GCP guidelines.

Hard Skills

  • Experience with Oncore, Excel, and Word
  • 2-3 years of clinical research coordinator experience in oncology
  • Experience in patient screening and study coordination

Soft Skills

  • Strong organizational skills
  • Excellent communication skills
  • Ability to anticipate needs of study sponsors

Work Site

This is a fully on-site position in Jersey City, New Jersey.

Work Environment

The position is based in Long Branch and Toms River with a dynamic team environment across various specialties including breast, lung, phase 1, and GI groups. The role is part of a large-scale operation with 100 FTEs, 5,000 subjects enrolled per year, and is involved in 300 active trials with a goal to expand further. The role requires interaction across multiple sites around the state.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are Embedded into our culture through:

  • Hiring diverse talent
  • Maintaining an inclusive environment through persistent self-reflection
  • Building a culture of care, engagement, and recognition with clear outcomes
  • Ensuring growth opportunities for our people

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email (see below) for other accommodation options.