20 Best Clinical Research Associate 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
13d
Clinical Research Coordinator I Registered Nurse
Novant Health —Charlotte, NC
Licensure/Certification: Current RN licensure in appropriate state, required. Additional Skills (preferred): Good Clinical Practice (GCP), Human Subjects…
Estimated: $57K - $72.2K a year
7d
Clinical Project Manager – Senior - Information Services Regional Strategic Projects
Indiana University Health —Indianapolis, IN
Facilitates current and future state clinical processes, requirements, elicitation, solutions and development and test management.
Estimated: $97.9K - $124K a year
Inhouse Clinical Research Associate
Novotech —United States
Relevant experience/qualifications in Life Sciences or related field or administration would be preferable. Update and maintain site milestones including EC/HA…
Estimated: $64.1K - $81.2K a year
Clinical Research Coordinator (CRC)-FT
Evolution Research Group —Columbus, OH
Manage studies with Principal Investigator, Site Director, and Recruitment Manager to develop effective programs for study enrollment.
Estimated: $49.3K - $62.4K a year
Quick Apply
Clinical Research Associate II
ProSciento, Inc —United States
Must be able to drive and have a valid driver’s license. University/college degree (life science preferred), or certification in a related allied health…
$100,000 - $125,000 a year
Quick Apply
Clinical Research Assistant/Medical Assistant
Alliance for Multispecialty Research, LLC —Lexington, KY
Assist in general office work flow which includes telephone answering. O Answering and triage of research office calls. O Filing and pulling study records.
From $20 an hour
Quick Apply
3d
Clinical Research Coordinator
Allegheny Health Network —Erie, PA
Driver's license may be required depending on facility requirements. Current research-related certification from accredited program such as The Association of…
Estimated: $52.9K - $67K a year
Clinical Research Associate
ProTrials Research, Inc. —United States
A valid driver's license with access to a car with up-to-date car insurance. Bachelor and/or advanced degree in biological sciences or related field, or…
$85,000 - $130,000 a year
23h
RN Clinical Research Coordinator - Full Time
Sanford Health —Fargo, ND
Currently holds an unencumbered RN license with the State Board of Nursing where the practice of nursing is occurring and/or possess multistate licensure if in…
$27.50 - $44.00 an hour
Quick Apply
7d
Postdoctoral Research Fellow/Associate - Brain Tumorigenesis
Cincinnati Children's Hospital Medical Center —Cincinnati, OH
Using mouse models, and state-of-the art cancer genomics, single-cell multi-omics, spatial transcriptomics, high-throughput drug and CRISPR/cas9 screens, as…
Estimated: $46.7K - $59.1K a year
Research Administrative Assistant
Colorado Urology Associates —Lakewood, CO
A High School Diploma is required; an associate's degree or equivalent experience in a relevant field is preferred. Schedule and manage research appointments.
$20 - $23 an hour
Quick Apply
19h
Clinical Research Associate
Sention Therapeutics, LLC. —San Diego, CA
The Clinical Research Associate is responsible for overall clinical site management, including site identification, feasibility, pre-study site evaluation,…
$140,000 - $190,000 a year
Quick Apply
Senior Clinical Data Manager
Celldex Therapeutics, Inc. —New Haven, CT
Initiate CRF development for new clinical trials and protocol amendments; collaborate with internal team and responsible vendor on CRF development, database…
Estimated: $124K - $157K a year
Clinical Manufacturing Associate II - Downstream
Rocket Pharmaceuticals —Cranbury, NJ
B.S./B.A. in Life Science, Biotechnology, ChemE, or a similar relevant field with 3+ years of experience in the pharmaceutical, biotech, or cell and gene…
Estimated: $64.9K - $82.2K a year
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
Quick Apply
Clinical Project Manager
Technical Resources International, Inc. —Bethesda, MD
Broad multidisciplinary understanding of the pharmaceutical clinical research and development processes with hands on regulatory, clinical operations, or…
Estimated: $106K - $134K a year
Clinical Research Coordinator/Medical Assistant
Alliance for Multispecialty Research, LLC —Layton, UT
Advise Investigator, Sub-Investigator and staff on protocols, procedures required for the successful implementation and completion of each clinical research…
$20 - $23 an hour
Quick Apply
4d
Clinical Project Associate (REMOTE)
Fresenius Medical Care —Meriden, CT
Review and comply with the Code of Business Conduct and all applicable company policies and procedures, local, state and federal laws and regulations.
Estimated: $77.7K - $98.4K a year
21h
Clinical Research Associate
Katalyst Healthcares & Life Sciences —United States
Participating in regional and global conference calls and meetings to review progress of ongoing clinical trials. Familiarity with EDC systems (i.e. Oracle).
Estimated: $68.3K - $86.5K a year
Quick Apply

I want to receive the latest job alert for Clinical Research Associate

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Senior Clinical Research Coordinator

Evolution Research Group - Staten Island, NY

Quick Apply

Job Details

$30 - $38 an hour 13 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

Quick Apply

Clinical Research Associate jobs

Senior Clinical Research Coordinator

Clinical Research Coordinator I Registered Nurse

Clinical Project Manager – Senior - Information Services Regional Strategic Projects

Inhouse Clinical Research Associate

Clinical Research Coordinator (CRC)-FT

Clinical Research Associate II

Clinical Research Assistant/Medical Assistant

Clinical Research Coordinator

Clinical Research Associate

RN Clinical Research Coordinator - Full Time

Postdoctoral Research Fellow/Associate - Brain Tumorigenesis

Research Administrative Assistant

Clinical Research Associate

Senior Clinical Data Manager

Clinical Manufacturing Associate II - Downstream

Senior Clinical Research Coordinator

Clinical Project Manager

Clinical Research Coordinator/Medical Assistant

Clinical Project Associate (REMOTE)

Clinical Research Associate

Job Seeker Tools

Employer Tools

Browse

Stay Connected