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
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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: $59.9K - $75.8K a year
12d
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: $107K - $135K 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
6d
Clinical Research Assistant
Alliance for Multispecialty Research LLC —Knoxville, TN
Assist in general office workflow which includes telephone answering. Answering and triage of research office calls. Filing and pulling study records.
$20 - $24 an hour
Quick Apply
Patient Recruitment & Clinical Research Associate
Piomic Medical AG —Remote
Participate and occasionally lead regularly scheduled update calls with study sites. Work closely with clinical team members to develop and fulfill patient…
$75,000 - $100,000 a year
Quick Apply
3d
Clinical Research Coordinator
NEXTSTAGE CLINICAL RESEARCH LLC —Waco, TX
The working environment consists of an indoor and climate-controlled setting the majority of the time, and with frequent exposure to a healthcare clinical…
$45,000 - $75,000 a year
Quick Apply
2h
Clinical Research Assistant/Medical Assistant
Alliance for Multispeciality Research, LLC —Kansas City, MO
Assist in general office workflow which includes telephone answering. O Answering and triage of research office calls. O Filing and pulling study records.
$21 - $23 an hour
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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
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9d
Clinical Research Coordinator
Alliance for Multispeciality Research —New Orleans, LA
Attach original document to certified copy before filing in the patient’s chart. Advise Investigator, Sub-Investigator and staff on protocols, procedures…
$24 - $27 an hour
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Clinical Trial Specialist
US Foot & Ankle Specialists —Cincinnati, OH
The CTS compiles and maintains project-specific status reports, interacts with the sponsor, study sites and internal associates, and provides oversight and…
Estimated: $55.5K - $70.3K a year
Quick Apply
Sr. Clinical Research Associate
Alimentiv —Remote
In-house based position, responsible for the design and oversight of project monitoring services including training, site/patient recruitment, site data…
$81,000 - $135,500 a year
Quick Apply
11d
Clinical Research Site Manager
Alliance for Multispeciality Research, LLC —Layton, UT
Hire, train and develop new team members to meet organizational needs. Provide timely feedback on employee performance, helping to develop a team members skill…
$90,000 - $95,000 a year
Quick Apply
9d
Clinical Research Coordinator
ObjectiveHealth —Akron, OH
The ideal candidate will possess certification such as an RN, LPN, MA, phlebotomy, or similar, prior clinical research experience, and have a strong desire to…
Estimated: $51.2K - $64.9K a year
Quick Apply
6d
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
3d
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: $45.8K - $57.9K a year
Quick Apply
Protocol Monitor (Clinical Research Associate)
The Jaeb Center for Health Research —Remote
A clinical research associate certificate is preferred. Protocol Monitors perform both remote and on-site monitoring and site management activities for clinical…
$70,000 - $85,000 a year
Quick Apply
5d
Clinical Trial Associate
Crinetics Pharmaceuticals —Remote
Physical Activities: On a continuous basis, sit at desk for a long period of time; intermittently answer telephone and write or use a keyboard to communicate…
$57,000 - $75,000 a year
Quick Apply
9d
Clinical Research Associate - Sponsor Dedicated
IQVIA —Remote
We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world.
Estimated: $65.5K - $82.9K a year
RESEARCH OPHTHALMIC ASSISTANT
Vance Thompson Vision Clinic Prof L —Sioux Falls, SD
Serving as the primary liaison between clinical study sponsors, patients, and VTV staff regarding study protocol requirements and communicates clinical study…
Estimated: $40.1K - $50.8K 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

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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Clinical Research Associate jobs

Senior Clinical Research Coordinator

Clinical Research Coordinator I Registered Nurse

Senior Clinical Data Manager

Clinical Research Associate

Clinical Research Assistant

Patient Recruitment & Clinical Research Associate

Clinical Research Coordinator

Clinical Research Assistant/Medical Assistant

Clinical Research Assistant/Medical Assistant

Clinical Research Coordinator

Clinical Trial Specialist

Sr. Clinical Research Associate

Clinical Research Site Manager

Clinical Research Coordinator

RN Clinical Research Coordinator - Full Time

Clinical Research Coordinator (CRC)-FT

Protocol Monitor (Clinical Research Associate)

Clinical Trial Associate

Clinical Research Associate - Sponsor Dedicated

RESEARCH OPHTHALMIC ASSISTANT

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