20 Best senior clinical research coordinator jobs (Hiring Now!)

Senior Clinical Research Coordinator
Evolution Research Group —Staten Island, NY
Manage studies with Principal Investigator, Site Director, and Recruitment Manager to develop effective programs for study enrollment.
$30 - $38 an hour
Quick Apply
12d
Weekend Clinical Coordinator, RN, HOME CARE, Part-time
Natick Walpole Visiting Nurse Association —Walpole, MA
Master’s Degree in a clinical field or MBA, preferred. Make welcome calls to new patients. Promotes compliance with all federal and state regulations.
Estimated: $61.7K - $78.1K a year
Quick Apply
12d
Senior Clinical Research Coordinator
Early Access Care LLC —Madison, CT
BS/BA, education required preferably in a health-related, life science area or technology-related field or equivalent combination of education, training, and…
$105,000 - $150,000 a year
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Social Work Clinical Care Coordinator
The Coordinating Center —Upper Marlboro, MD
If you are a registered nurse (RN) or licensed social worker (LMSW, LCSW-C) and have experience in case management/care coordination, home health, school…
Estimated: $59.9K - $75.9K a year
10d
Assistant Clinical Care Coordinator - LVN
Sisters of the Holy Names —Campbell, CA
Valid drivers' license and personal vehicle. Enhances each Sister’s understanding of her own medical needs. Thorough knowledge and understanding of the concepts…
$38 - $41 an hour
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14d
Clinical Care Coordinator
Legacy Medical —Rapid City, SD
This position is responsible for assisting Nurse Practitioners and Physician Assistants care for senior patients in Assisted Living and home environments.
Estimated: $38K - $48.1K a year
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RN Clinical Care Coordinator
The Coordinating Center —Upper Marlboro, MD
If you are a registered nurse (RN) or licensed social worker (LMSW, LCSW-C) and have experience in case management/care coordination, home health, school…
Estimated: $65.8K - $83.3K a year
10d
Senior Clinical Research Coordinator
Northwell Health —Lake Success, NY
Uses statistical software to analyze study data and interface with biostatisticians for analysis; engages physician leaders from various specialties to develop…
$58,540 - $92,650 a year
18h
Clinical Nurse Coordinator Intermediate Care Unit
Wesley Medical Center —Wichita, KS
Current Kansas Registered Nurse License or valid compact license. Education assistance (tuition, student loan, certification support, dependent scholarships).
Quick Apply
5h
Principal/ Sr. Scientist- Dermal Clinical Research
Colgate-Palmolive —Piscataway, NJ
Identify and help develop new innovative clinical methods to explore new technical leads, active ingredients and product claims substantiation.
Senior Clinical Administrative Coordinator - Remote in EST
Optum —Tampa, FL
Notify Care Team of relevant information gathered during calls to patient that may affect the patient’s disease state or medication regimen.
$19.47 - $38.08 an hour
2d
Senior Clinical Research Associate - CNS - Northeast
Worldwide Clinical Trials —Pennsylvania
Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study…
Estimated: $78.8K - $99.8K a year
Quick Apply
Senior Clinical Research Associate
ProTrials Research, Inc. —United States
RN or Bachelor and/or advanced degree in biological sciences or related field, or equivalent combination of relevant experience, education or training, and…
$115,000 - $140,000 a year
21h
Clinical Team Coordinator RN - Cardiac Special Care Unit
Geisinger —Scranton, PA
Assists in developing, initiating, and supporting improvements, on the unit level, that facilitate the delivery of high quality, safe and cost-effective patient…
Senior Clinical Research Associate
Novartis —Remote
Collaborates with internal stakeholders and site personnel to manage data query resolution process to ensure timely and accurate data entry.
$112,800 - $169,200 a year
7d
Clinical Nurse Coordinator Critical Care ICU RN
Methodist Hospital Westover Hills —San Antonio, TX
Education assistance (tuition, student loan, certification support, dependent scholarships). Whether you choose to focus on bedside care, a leadership or C…
Quick Apply
9d
Clinical Research Associate/Senior Clinical Research Associate
Edgewise Therapeutics —Remote
The assigned clinical trials will be highly complex and high risk, e.g., multiple indications, data monitoring committees, interim analyses, adaptive design,…
$75,000 - $145,000 a year
Quick Apply
Senior Clinical Research Associate - Oncology - West Coast
Worldwide Clinical Trials —California
Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study…
Estimated: $84.4K - $107K a year
Quick Apply
11d
Senior Clinical Administrative Coordinator - National Remote
UnitedHealth Group —Dallas, TX
Manage the referral process, processing incoming and outgoing referrals and prior authorizations, including intake, notification and census roles.
$19.47 - $38.08 an hour
13d
Senior Clinical Research Associate
Catalyst Clinical Research LLC —Remote
As a Senior Clinical Research Associate, you will monitor clinical trial programs and manage regional clinical trial sites to support biological and…
Estimated: $118K - $149K a year
Quick Apply

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Senior Clinical Research Coordinator

Evolution Research Group - Staten Island, NY

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Job Details

$30 - $38 an hour 12 days ago

Qualifications

Microsoft Excel
Clinical research
11+ years
High school diploma or GED
Computer skills
Medical terminology
Communication skills
FDA regulations

Full Job Description

Title: Senior Clinical Research Coordinator

Location: Staten Island, NY

About us:

ERG is a leading U.S. based, privately held, independent clinical research site company, and provider of clinical development services with expertise in early and late-stage neuroscience drug development. With 20 wholly owned clinical sites and 4 affiliated sites, we conduct in-patient and out-patient phase I-IV clinical research studies. ERG has 400+ in-patient beds, a large and growing database of patients suffering from mental illness, neurological disorders, sleep disorders, addictions, Acute and Chronic Pain, diabetes, and other illnesses as well as normal healthy volunteers who participate in trials for the advancement of medicine. With access to over 32 million patients/subjects and 5000 + completed trials, ERG continues to grow its capabilities and expand into indications where there are tremendous unmet medical needs in the United States and globally.

Job Description:

The Clinical Research Coordinator V or Senior Clinical Research Coordinator will complete all study related procedures and distribute study medication and instructions to research subjects under the direction of the Principal Investigator and the Site Director. They will maintain accurate, confidential files and documentation of study participants. In executing these position responsibilities, the Clinical Research Coordinator is guided by FDA regulations, Good Clinical Practice (GCP), and company standard operating procedures and policies.

Responsibilities:

General

Obtain detailed knowledge of all components of each study protocol through review and analysis of study information with Principal Investigator and Site Director prior to the effective date of the study.
Act as head coordinator responsible for supervising and coordinating others working on protocols and interfacing with CRA and company personnel assigned to that study.
Assist Site Director with marketing activities where appropriate.
Develop draft source documents and review the documents for accuracy and clarity prior to study start up.
Develop a mechanism for subject recruitment and ongoing communications with PCP and nursing staff as appropriate.
Review with Principal Investigator and Site Director, any components of the study for which additional information or clarification are required prior to the initiation of the study.
Organizational management of all aspects of the trial, including but not limited to caseload and study files.
Manage studies with sponsor, and Principal Investigator to ensure compliance with protocol requirements.
Manage studies with Principal Investigator, Site Director, and Recruitment Manager to develop effective programs for study enrollment.
Serve as a mentor and trainer for support staff and new employees once the Clinical Research Coordinator has been approved to do so by the Site Director.
Contribute to the SOP review and development as delegated by the Site Director.
Communication of all protocol related issues/problems to the appropriate management staff, including but not limited to questions regarding the conduct of the clinical trial.

Study Management

Perform study activities as delegated by the Principal Investigator and under the supervision of the Site Director.
Attend the investigator meeting for each assigned protocol, as appropriate.
Completion of IRB study renewals and maintain copies of all IRB communications.
In conjunction with Site Director and Principal Investigator, ensure adherence to the protocols and document breaches or violations with sponsors and appropriate Institutional Review Boards (IRBs) and other outside regulatory organizations, as required.
Screen, enroll subjects and schedule subject visits in conjunction with Principal Investigator
Review and obtain informed consent from with potential study volunteers.
Document all written and phone correspondences with sponsor, labs, IRB other regulatory organizations.
Maintain organized, accurate and complete study records including but not limited to regulatory documents, signed informed consents, IRB correspondence/approvals, source documentation, drug dispensing logs, subject logs and study-related communications.
Assist Principal Investigator in conducting studies in manner to ensure integrity of data and safety of subjects.
Enter data as appropriate for protocol (paper-electronic data capture)
Ensure timely and accurate CRF completion for each study subject.
In conjunction with Principal Investigator, accurately report and track adverse events as defined by each study protocol.
Outcomes of enrollment and sponsor monitoring visits of all assigned protocols
Perform study close-out procedures.
Additionally, this role may encompass responsibilities beyond those outlined above, as required by the evolving needs of the organization. This job description is intended as a foundation and may be subject to expansion or modification to best suit ERG’s objectives.

Skills and Qualifications:

Education and experience
- High School Diploma or its equivalent; College degree preferred.
- Fourteen (14) plus years of experience as a Clinical Research Coordinator
- Understands regulatory requirements, as well as Good Clinical Practices (GCP) and International Conference on Harmonization (ICH) guidelines.
- Certified as a coordinator.
- Able to communicate with providers, co-workers, sponsors, and others in a collaborative and courteous manner.
- Knowledgeable in medical terminology to communicate with physician office and laboratory staff.
- Demonstrate the initiative to act independently, initiating activity as required and making appropriate decisions within the constraints of study protocols, regulatory requirements, and company policy.
- Able to initiate or modify behavior to achieve desired outcomes despite environmental factors, priorities, or problems that might not be well defined or that are subject to change.
Requirements
- Understand regulatory requirements, as well as Good Clinical Practices (GCP) and International Conference of Harmonization (ICH) guidelines.
- Knowledgeable in medical terminology
- Excellent communication skills (interpersonal, written, verbal)
- Basic computer skills to include Word, Excel, as well as proprietary applications unique to the clinical research industry (such as Study Manager)

#MedHP

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senior clinical research coordinator jobs

Senior Clinical Research Coordinator

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Senior Clinical Research Coordinator

Social Work Clinical Care Coordinator

Assistant Clinical Care Coordinator - LVN

Clinical Care Coordinator

RN Clinical Care Coordinator

Senior Clinical Research Coordinator

Clinical Nurse Coordinator Intermediate Care Unit

Principal/ Sr. Scientist- Dermal Clinical Research

Senior Clinical Administrative Coordinator - Remote in EST

Senior Clinical Research Associate - CNS - Northeast

Senior Clinical Research Associate

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Senior Clinical Research Associate

Clinical Nurse Coordinator Critical Care ICU RN

Clinical Research Associate/Senior Clinical Research Associate

Senior Clinical Research Associate - Oncology - West Coast

Senior Clinical Administrative Coordinator - National Remote

Senior Clinical Research Associate

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