Top 19 Clinical research Jobs in Boise Id

Clinical Research Coordinator
Paradigm Clinical Research Center —Boise, ID
- $55,000 - $65,000 a year
- Full-time
- Background check
- Mid-level
- Master's degree
- Health insurance
- Dental insurance
Quick Apply
Clinic Research Coordinator - MA
IDAHO GASTROENTEROLOGY ASSOCIATES, LLP —Meridian, ID
- Full-time
- Bilingual
- BLS Certification
- Mid-level
- Paid jury duty
- Paid holidays
14d
Sr CRA (Level I) - FSP - Oncology (Central/West Coast)
Thermo Fisher Scientific —Idaho
- Full-time
- RN License
- Computer literacy
- Writing skills
6d
Clinical Research Coordinator (CRC/CCRC)
High Desert Heart and Vascular —Meridian, ID
- Full-time
- Nursing
- Ability to walk for extended periods
- Computer literacy
Quick Apply
8d
Senior Clinical Research Associate - US - Oncology
Worldwide Clinical Trials —Boise, ID
- $97,000 - $193,000 a year
- Full-time
- Nursing
- 5 years
- English
Trauma Certified Data Registrar
St. Luke's Health System —Meridian, ID
- Full-time
- Remote
- Mid-level
- High school diploma or GED
- Paid time off
Quick Apply
3d
Staff Psychologist-PTSD Clinical Team Psychologist and Outpatient Substance Use Disorder Specialist
US Veterans Health Administration —Boise, ID
- $78,040 - $144,599 a year
- Online Application
- Background check
- Doctoral degree
- Writing skills
- Paid parental leave
- Paid holidays
Physician: Pediatric Clinical Oncology
St. Luke's Health System —Boise, ID
- Full-time
- BC/BE
- Inpatient
- Children
Quick Apply
Post Doctoral Research Fellow
Boise State University —Boise, ID
- $55,057.60 - $65,000.00 a year
- Temporary
- University
- Doctor of Philosophy
- US work authorization
- Paid holidays
- Health insurance
Special Agent: Healthcare Services/Medical Background
Federal Bureau of Investigation —United States
- $103,326 - $133,200 a year
- Full-time
- Research
- Mid-level
- Bachelor's degree
MedTech Part Time Clinical Consultant – East Bay, San Francisco, CA
IQVIA —United States
- $85 an hour
- Part-time
- RN License
- Mid-level
- 3 years

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Inside Sales Representative
IQVIA —Boise, ID
Initiates and answers inbound and/or outbound sales calls or electronic inquiries directly from/to prospective and/or existing customers.
$32.00 - $34.62 an hour
MedTech Part Time Clinical Consultant – East Bay, San Francisco, CA
IQVIA —United States
Must provide a minimum of (2) days of live support within the field (case support, patient rounding, providing education), with a total of (5) days of…
$85 an hour

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Clinical Research Coordinator-Clinical Trials Management Office
The Ohio State University Wexner Medical Center —Columbus, OH
Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the non-cancer…
3d
Clinical Research Coordinator
OhioHealth —Columbus, OH
This position performs basic day to day activities related to clinical research studies including recruit and screen participants, obtains informed consent,…

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Clinical Research Coordinator

Paradigm Clinical Research Center -
Boise, ID

Quick Apply

Job Details

Full-time
$55,000 - $65,000 a year

Benefits

Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance

Qualifications

Clinical research
Phlebotomy
Organizational skills

Full Job Description

Overview
We are seeking a dedicated and detail-oriented Clinical Research Coordinator to join our team. This role is integral to the successful execution of clinical trials, ensuring that all research activities are conducted in compliance with regulatory standards and Good Clinical Practice (GCP). The ideal candidate will have a strong background in clinical research and possess excellent organizational skills to manage various aspects of study coordination.

Responsibilities

Coordinate clinical research studies from start to finish, including study start-up, recruitment, screening, enrollment, treatment, follow-up, and close-out.
Develop and maintain study documents, including study protocols, informed consent forms, case report forms, and study manuals.
Obtain and maintain regulatory approvals, including Institutional Review Board (IRB) approvals and other required regulatory documentation.
Screen and enroll eligible study participants according to study protocols and ensure that participants receive appropriate study treatments and follow-up care.
Collect and manage study data using electronic data capture systems and ensure the accuracy and completeness of study data
Develop and maintain study databases, conduct quality control checks, and generate study reports as required.
Work closely with study sponsors and other stakeholders to ensure the successful completion of clinical research studies.
Train and supervise research staff, including research assistants and volunteers, and ensure compliance with study protocols and regulatory requirements.
Communicate study progress and results to study sponsors, regulatory authorities, and other stakeholders.
Participate in the development and implementation of new clinical research studies and initiatives.
Coordinate study activities with other departments and external partners.
Monitor study progress and works to identify research related issues and discrepancies when evident, and appropriately escalates to site manager, director, or investigator for resolution as needed.
Ensure compliance with study protocols, GCP guidelines, and regulatory requirements.
Train and supervise junior research staff as required.
Assist with collecting training forms, collection and or preparation of essential documents and obtaining required signatures from all applicable research personnel for regulatory/essential documents throughout the duration of a study including, but not limited, to Food and Drug administration (FDA) form 1572, CV, professional licensure, financial disclosure form (FDF), and Institutional Review Board (IRB) submission forms.
Communicate with study participants and their families to provide study-related information and to ensure study visit schedules are met.
Adheres to standard operating procedures (SOP).
Participate in study team meetings and attend required training and educational sessions.
Maintain study supplies and equipment and ensure that they are stored and maintained in accordance with regulatory requirements.
Trains under the guidance of direct supervisor and other site personnel to promote participation in research studies including mail-outs and other marketing programs as applicable.
Assist with general managed site projects and workload sharing as assigned by direct supervisor.

Experience

CCRC Required.
Bachelor or master’s degree in a health-related field such as biology, or public health
preferred.
Proficient knowledge of GCP guidelines, regulatory requirements, and clinical trial
operations
> 4 years’ experience working in clinical research environment.
Excellent organizational and communication skills.
Ability to work independently and as part of a team.
Strong organizational skills and attention to detail, with the ability to manage multiple tasks and priorities simultaneously.
Excellent communication skills, with the ability to communicate effectively with study sponsors, regulatory authorities, research staff, and study participants.
Proficient in the use of electronic data capture systems and database management tools.
Ability to work independently and as part of a team in a fast-paced, deadline-driven environment.
Willingness to learn new skills and take on new responsibilities as needed.

If you are passionate about advancing medical research and have the necessary skills to excel as a Clinical Research Coordinator, we encourage you to apply for this exciting opportunity.

Job Type: Full-time

Pay: $55,000.00 - $65,000.00 per year

Benefits:

401(k)
Dental insurance
Health insurance
Paid time off
Vision insurance

Ability to Commute:

Boise, ID 83709 (Required)

Work Location: In person

Quick Apply

Refine Your Search

clinical research jobs in boise id

Clinical Research Coordinator

Clinic Research Coordinator - MA

Sr CRA (Level I) - FSP - Oncology (Central/West Coast)

Clinical Research Coordinator (CRC/CCRC)

Senior Clinical Research Associate - US - Oncology

Trauma Certified Data Registrar

Staff Psychologist-PTSD Clinical Team Psychologist and Outpatient Substance Use Disorder Specialist

Physician: Pediatric Clinical Oncology

Post Doctoral Research Fellow

Special Agent: Healthcare Services/Medical Background

MedTech Part Time Clinical Consultant – East Bay, San Francisco, CA

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