Clinical Research Specialist jobs in United States
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Dignity Health ยท 1 day ago

Clinical Research Specialist

Dignity Health is seeking a Clinical Research Specialist to join the Gregory W. Fulton ALS and Neuromuscular Disease Center team in Phoenix, AZ. The role involves ensuring compliance with regulatory requirements, assisting in participant recruitment, coordinating research activities, and providing education to participants.

Health CareHospitalMedicalNon Profit
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H1B Sponsor Likelynote

Responsibilities

Ensures assigned studies are conducted in accordance with the Food and Drug Administration (FDA) Office for Human Research Protections (OHRP) Good Clinical Practices (GCP) Institutional Review Board (IRB) HIPAA regulations and institutional requirements which include but are not limited to the following duties:
Knowledge of regulatory requirements and institutional requirements when conducting study protocol(s)
Assists with participant recruitment including pre-screening potential participant follow-up and collaboration with Investigators
With the Investigators coordinates research subject informed consent and enrollment into appropriate research studies
Coordinates and/or performs a variety of procedures/tests including but not limited to laboratory tests/phlebotomy vital signs ECG outcomes assessments cognitive evaluations as well as other needs as outlined in the study protocol(s)
Obtains medical history medical records and all other procedures outlined in the study protocol(s) within the allowed timelines
Responds to patient inquiries via phone or in person in a timely manner
Processing and shipment of laboratory samples collected as outlined in the study protocol(s)
Provides participant education with the Investigators research pharmacists and other members of the research study team such as study specific procedures diary/study log proper dosage/administration and specific restrictions as outlined in the study protocol(s)
Completes case report forms data entry and maintains source documentation for all study participants
Prepares for participant visits including scheduling and source document creation
Triages tracks and reports adverse events and deviations to the Investigator as well as the sponsor and IRB in accordance to their requirements
Coordinates research monitor visits and responds to all data queries in a timely manner

Qualification

Clinical research experienceGCPRegulatory complianceMicrosoft Office proficiencyParticipant recruitmentData entryPatient communicationInformed consent coordination

Required

Minimum 2 Years Related Experience Required
Competent in computer skills including the Microsoft Office products required
Associates degree in related field or an equivalent combination of relevant education and/ or job-related experience in lieu of degree required

Preferred

Three (3) years clinical research experience preferred
Bachelors Degree in related field preferred

Company

Dignity Health

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Dignity Health is a healthcare facility that offers physical, mental, and spiritual care.

H1B Sponsorship

Dignity Health has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (44)
2024 (55)
2023 (38)
2022 (37)
2021 (33)
2020 (20)

Funding

Current Stage
Late Stage
Total Funding
unknown
2019-02-01Acquired

Leadership Team

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Gena Bravo
President/CEO
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Linda Tautz RN, BSN, MBA
Regional Chief Executive Officer
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Company data provided by crunchbase