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IQVIA
Overview
The Clinical Research Associate will monitor and manage clinical trial sites to ensure strict adherence to study protocols, GCP/ICH guidelines, and regulatory requirements. Responsibilities include conducting site visits, overseeing recruitment plans, managing documentation, and providing training to site staff.
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Compensation
$71,900 - $189,000 / YEAR
Posted
2 days ago
University of Iowa
Manage and support clinical trial regulatory activities for the Pediatric Department, including IRB submissions and documentation. Act as a back-up study coordinator to assist with subject visits, data entry, and protocol execution.
Salary not listed
4 days ago
Iterative Health
The Clinical Research Coordinator I supports and coordinates daily clinical trial activities, including administratively and clinically managing industry-sponsored trials, problem-solving, and ensuring protocol adherence. Key duties involve leading patient recruitment, scheduling visits, conducting procedures like blood draws and injections, and dispensing study medication.
K2 Staffing LLC
The Clinical Research Assistant supports clinical trial performance by managing candidate screening and maintaining accurate source documentation. They perform clinical tasks including phlebotomy and ECGs while ensuring strict adherence to study protocols and federal regulations.
9 days ago
Kahak Health
Serve as a supportive household member and mentor for individuals with intellectual and developmental disabilities within a home environment. Provide assistance with daily living activities, community integration, and skill-building to promote independence.
10 days ago
Provide a safe and supportive home environment for individuals with intellectual and developmental disabilities. Assist with daily living activities, community integration, and skill-building while following Individualized Service Plans.
LifeStance Health
Provide comprehensive mental healthcare to adults in an outpatient setting through both medication management and therapy. Collaborate with mid-level providers to ensure high-quality, evidence-based clinical outcomes.
$395,000 - $435,000 / YEAR
University of Pennsylvania
The role involves coordinating complex oncology clinical trials, ensuring protocol execution according to GCP and HIPAA standards. Responsibilities include managing patient visits, handling regulatory submissions, and maintaining audit-ready study files.
$53,418 - $60,813 / YEAR
University of Pennsylvania Perelman School of Medicine
Coordinate and execute oncology clinical trials in accordance with GCP and HIPAA regulations. Manage patient eligibility, data collection, regulatory documentation, and biological sample processing.
Perform site monitoring and management to ensure study protocols, regulatory requirements, and GCP/ICH guidelines are strictly followed. Manage study progress by tracking regulatory submissions, recruitment, data integrity, and site documentation.
$71,900 - $169,300 / YEAR
Headlands Research
The Sub-Investigator will ensure the safety and welfare of study subjects by maintaining in-depth knowledge of all research protocols, screening subjects, conducting medical interviews and exams, reviewing results, and providing necessary medical care during trials. Responsibilities also include providing home-based on-call availability and attending Investigator Meetings when required.
Profound Research
Coordinate high-volume vaccine clinical trials by managing participant visits, performing clinical procedures, and maintaining audit-ready documentation. Collaborate with investigators, sponsors, and CROs to ensure compliant and efficient trial execution from start-up to closeout.
11 days ago
Coordinate high-volume vaccine clinical trials by managing participant visits, performing clinical procedures, and maintaining audit-ready documentation. Collaborate with investigators, sponsors, and CROs to ensure compliant and high-quality trial execution from start-up to closeout.
Flourish Research
The Clinical Research Coordinator serves as the primary contact for study participants and sponsors, ensuring participant safety and accurate data collection. Key duties include obtaining informed consent, managing study medications, and coordinating laboratory specimens according to protocol.
$26 - $34 / HOUR
14 days ago
Trinity Health
The role involves assisting with patient care and supporting residents in a healthcare setting. Successful candidates will also participate in a paid CNA training program.
$18 / HOUR
16 days ago
University of Miami
The Sponsored Program Specialist monitors, supports, and evaluates grant activities to ensure compliance with guidelines and regulations. They manage research funding, prepare grant proposals, review awards, and maintain accurate records.
Ally Psychiatry
Perform psychiatric evaluations, diagnostic assessments, and medication management for outpatient patients. Collaborate with a multidisciplinary team of PMHNPs and therapists while supervising advanced practice providers.
The Psychiatrist will join an outpatient clinic in Gadsden, Alabama, providing psychiatric care and collaborating with experienced mid-level providers. This role involves a standard call rotation consistent with other providers within the organization.
Participate in a paid training program to earn a Certified Nurse Assistant certification. Provide compassionate, person-centered care to residents in a healthcare setting upon completion of the program.
17 days ago
Tandem Intermediate LLC
The Clinical Research Nurse oversees daily study activities and ensures all procedures follow protocol guidelines. Responsibilities include collecting patient data, performing clinical tasks, and maintaining communication between investigators, sponsors, and patients.
22 days ago
