20 Best Clinical Research Associate jobs (Hiring Now!)

Clinical Research Site Manager
Texas Diabetes & Endocrinology, P.A. —Round Rock, TX
This person will answer staff questions regarding clinical trials and general office concerns. Provides a safe environment for patients, families, and clinical…
From $50,671.80 a year
Quick Apply
Clinical Research Coordinator, RN
Wichita Urology Group —Wichita, KS
The CRC will develop, implement, and coordinate research and administrative procedures for the successful management of clinical trials.
From $50,000 a year
Quick Apply
5d
Clinical Research Coordinator
NEXTSTAGE CLINICAL RESEARCH LLC —Waco, TX
This position requires frequent sitting, walking, standing, reading, seeing, speaking, hearing, listening, organizing, interpreting data and information,…
$45,000 - $75,000 a year
Quick Apply
8d
Experienced Clinical Research Coordinator
California Liver Research Institute —Pasadena, CA
The CRC will develop, implement, and coordinate research and administrative procedures for the successful management of clinical trials.
From $25 an hour
Quick Apply
Oncology Clinical Research Associate - IQVIA Biotech
IQVIA —Remote
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and…
$87,200 - $145,300 a year
1h
Clinical Research Coordinator
CenExel iResearch —Decatur, GA
Bachelor's Degree or equivalent experience in Clinical Research or related field. O Responsible for timely data entry and query resolution.
Estimated: $45.8K - $58K a year
Quick Apply
GME Research Coordinator
Northeast Georgia Health System —Gainesville, GA
Minimum Experience: Minimum of five years experience in healthcare research, public health research and/or academic science or PhD in related area, and evidence…
Estimated: $80.8K - $102K a year
Clinical Research Assistant
Colorado Springs Urological Associates PLLC —Spokane, WA
Take telephone messages and provided feedback and answers to patient/pharmacy/physician calls. Professional attitudes sufficient to demonstrate honest, ethical…
$20 - $27 an hour
Quick Apply
12d
RN Clinical Research Coordinator - Phase 1 Oncology - Full Time
Sanford Health —Sioux Falls, SD
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
12h
Sr. Clinical Research Associate
Avania —United States
Avania’s ClinOps Team establishes, maintains and supports clinical trials; as a key member of the team, our Sr CRA performs clinical trial oversight for the…
Estimated: $94.6K - $120K a year
Quick Apply
6d
Clinical Research Coordinator
Tandem Clinical Research —Albany, NY
Maintain required records of study activity including source documentation, case report forms, drug dispensation records, and data management system entry.
From $55,000 a year
Quick Apply
4d
Clinical Research Coordinator
Quality Clincial Research —Omaha, NE
Work closely with the Principal Investigator and other team members to develop and implement research protocols. Clinical research: 1 year (Required).
$26 - $30 an hour
Quick Apply
7d
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 Research Coordinator
cCARE —Fresno, CA
Possesses a thorough knowledge of the informed consent process as well as a thorough understanding of the study protocol(s) in order to be able to answer all…
$25 - $32 an hour
Quick Apply
Clinical Research Coordinator - Gastroenterology Practice
GI Specialists of Georgia —Marietta, GA
Assists the PI in development of materials and tools necessary to appropriately train individuals involved in the conduct of the study around issues related to …
$26 - $30 an hour
Quick Apply
Clinical Research Coordinator
CARE Institute —Boise, ID
Interacts professionally with trial compliance monitors, answering all queries & making necessary corrections if applicable..
$20 - $24 an hour
Quick Apply
4d
Research Associate - Orthopedic Research - CORIT Lab
UTHealth Houston —Houston, TX
May recruit study participants or field interviewers. Bachelor’s degree in a related field with three (3) years of related research experience including…
Estimated: $51.3K - $65K a year
Site Manager-Dorchester, MA
Care Access —Dorchester, MA
Act as a primary point of contact in the therapeutic field for Care Access Research. Ability and willingness to mentor and guide less experienced CRC as they…
Estimated: $89.2K - $113K a year
Quick Apply
Clinical Research Coordinator (local recruits only)
Las Vegas Medical Research —Las Vegas, NV
Collaborating closely with principal investigators to coordinate all aspects of research studies, from participant recruitment and eligibility assessment to…
$27 - $33 an hour
Quick Apply
Business Attraction and Investment Manager, CRA
City of Dania Beach —Dania Beach, FL
If the driver’s license is out of state, must be able to obtain a Florida driver’s license within thirty (30) days of the hire date.
$66,181.32 - $102,580.95 a year

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Clinical Research Site Manager

Texas Diabetes & Endocrinology, P.A. - Round Rock, TX

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Job Details

Full-time From $50,671.80 a year

Benefits

Health savings account
Health insurance
Dental insurance
401(k)
Paid time off
Employee assistance program
Vision insurance
Life insurance
Referral program

Qualifications

CPR Certification
CCRC
LVN
RN License
Research
Supervising experience
Bachelor's degree
Patient care
Clinical trials
CCRP
Associate's degree
Endocrinology
Medical terminology
2 years
AED Certification
FDA regulations

Full Job Description

Texas Diabetes & Endocrinology, P.A. (TD&E) has grown over the years to meet the Endocrinology needs of the Austin community. Our mission is to strive to provide expert care in Diabetes, Thyroid problems, Osteoporosis, Weight management and hormonal conditions by providing thorough evaluations and innovative, personalized solutions focused on our patients success. Our employees are the strength that keeps us moving forward.

Our Clinical Research Department is looking for a Clinical Research Site Manager for our Round Rock Office!

Purpose: The Clinical Research Site Manager is responsible for overseeing the daily operations of the Clinical Research Department at their location including the adherence to Standard Operations Procedures, Good Clinical Practice, and FDA regulations. In support of the Clinical Research Coordinators (CRC) and Assistant Clinical Research Coordinators (ACRC), the Site Manager will have advanced knowledge of ongoing clinical studies including protocols and titration algorithms. This includes but is not limited to ensuring proper clinical trial protocol procedures are always followed to obtain the correct data, working with investigators to schedule patient procedures and sponsor meetings, keeping patient charts always organized, and communicating with sponsors with updates on patient data. This person will answer staff questions regarding clinical trials and general office concerns. The Site Manager will work together with the Director of Site Operations on departmental staffing, terminations, performance reviews, and disciplinary actions. This position may manage clinical trials as needed.

Essential Functions:

Oversees the daily operations of the research department at location while supporting the Director of Site Operations with other location operations on a backup basis.
Manages and mentors CRCs on day-to-day activities at the site. Handles staffing, performance management, and disciplinary actions with the support of the Director of Site Operations. Ensures staff and direct reports are appropriately trained and supported to enable their success. Approves timesheets and leave requests in Paycom.
Maintains advanced knowledge of all ongoing clinical trials. Provides oversight and coordination in support of CRC and ACRC, and ensures effective end-to-end planning, execution, and close out of trials.
Reviews site regulatory documents such as informed consents, Institutional Review Board (IRB) approvals, and research agreements to ensure compliance with study requirements. Participates in IRB audits.
Oversees interactions with CRCs and sponsors, including Monitor Visits.
Manages project plans and resources to ensure compliance with protocols and contracts. Maintains an overview of clinical trials’ operational status or risks and proactively communicates the progress and issues to the PI or Sponsor as applicable.
Serves as the point of contact for research department issues at location. Reports any major issues to the Director of Site Operations and/or Director of Business & Finance and/or Investigators.
Understands serious adverse events and reporting requirements of clinical trials. Works with the staff to review medical records and ensure all relevant SAE information is reported.
Interacts with Director of Site Operations and/or Investigators as needed to ensure patient receives appropriate medical evaluation and care when needed. Alerts Director of Site Operations of serious adverse events.
Is responsible for ensuring completion of all study source documentation for studies at the site, including case report forms and other study specific documents.
May manage clinical trials as needed, including providing support to CRC:
Attends sponsor Investigator/Study Coordinator meetings as needed for assigned protocols. Interacts with and maintains close communication with the sponsor’s Clinical Research team.
Coordinates and conducts patient care visits including but not limited to drawing blood, collecting vital signs, performing EKG’s, processing specimens, and ensuring all procedures are conducted in compliance with the clinical protocol. Ensures the processing of any lab work and proper shipment.
Partners with providers to coordinate checkup and documents patient updates post visit.
Trains patients on how to use pump/incline meter and on potential side effects of medications.
Oversees sponsors’ database clean-up process.
Ensures payments to patients are processed and works with the Director of Business & Finance to manage all patient payments.
Attends / leads provider meetings regarding ongoing and potential clinical trials.
Leads research meetings with site staff including creating the agenda.
Assists the Recruitment Manager with recruitment meetings as applicable and plays a big part in driving the recruitment at their site. Sends regular recruitment updates to site staff and investigators. Is always aware of recruitment needs.
Keeps after-hours phone as needed.
Provides a safe environment for patients, families, and clinical staff at all times through compliance with all federal, state, and professional regulatory standards as issued through OSHA and the CDC. Maintains strict patient confidentiality according to HIPAA regulations and applicable law.

Additional Non-Essential Functions:

Other duties as assigned.

Education & Experience Requirements:

Minimum Required:

Minimum 2 years of prior Clinical Trials experience
Knowledge of research methodology, medical terminology, and pharmacology
CCRC or CCRP Certification required after qualifying hours met per the ACRP

Preferred:

Associates/Bachelor’s Degree or equivalent in a scientific heath field/experience
Prior experience as CRC in a team lead or supervisory capacity
Experience in Diabetes and/or Endocrine or Pharmaceuticals Clinical Trials
Prior experience in a patient care role such as MA, LVN, or RN with phlebotomy
CPR/AED Certification

This position will require CCRC or CCRP certification after meeting all Association of Clinical Research Professional (ACRP) CCRC or CCRP hours.

AAP/EEO Statement

Texas Diabetes & Endocrinology, P.A. (TDE) provides equal employment opportunities (EEO) to all employees and applicants for employment in accordance with applicable federal, state, and local laws. TDE complies with applicable state and local laws governing nondiscrimination in employment in every location in which it has facilities.

Other Duties

Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.

Job Type: Full-time

Pay: From $50,671.80 per year

Benefits:

401(k)
Dental insurance
Employee assistance program
Health insurance
Health savings account
Life insurance
Paid time off
Referral program
Vision insurance

Experience level:

2 years

Schedule:

Day shift
Monday to Friday
No weekends

Ability to Commute:

Round Rock, TX 78681 (Required)

Ability to Relocate:

Round Rock, TX 78681: Relocate before starting work (Required)

Work Location: In person

Quick Apply

Clinical Research Associate jobs

Clinical Research Site Manager

Clinical Research Coordinator, RN

Clinical Research Coordinator

Experienced Clinical Research Coordinator

Oncology Clinical Research Associate - IQVIA Biotech

Clinical Research Coordinator

GME Research Coordinator

Clinical Research Assistant

RN Clinical Research Coordinator - Phase 1 Oncology - Full Time

Sr. Clinical Research Associate

Clinical Research Coordinator

Clinical Research Coordinator

Senior Clinical Research Coordinator

Clinical Research Coordinator

Clinical Research Coordinator - Gastroenterology Practice

Clinical Research Coordinator

Research Associate - Orthopedic Research - CORIT Lab

Site Manager-Dorchester, MA

Clinical Research Coordinator (local recruits only)

Business Attraction and Investment Manager, CRA

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