Clinical Research Associate Jobs in Wisconsin, United States

Clinical Research Associate (CRA) in Cell Therapy at AstraZeneca oversees study delivery at sites in Chicago or Wisconsin. Works with local study teams, monitors compliance with ICH‑GCP, GMP/GDP, and local regulations.

Clinical Research Associate II on the PPD Development team at Thermo Fisher Scientific, driving clinical monitoring and site management for oncology and ophthalmology trials. The role conducts remote and on‑site visits, applies risk‑based monitoring, ensures protocol compliance, and collaborates with investigators to maintain audit readiness.

Clinical Research Associate on Georgetown University’s Medical Center team, driving infectious disease trials by monitoring patients, administering investigational therapies, and ensuring protocol compliance. Day‑to‑day duties include data capture, regulatory documentation, and cross‑functional collaboration with the Clinical Trial Office, Pharmacy, and research coordinators.

IQVIA’s Clinical Research team builds and monitors clinical trials to accelerate medical innovation. The Clinical Research Associate conducts site monitoring visits, manages regulatory submissions, and ensures protocol compliance across multiple study sites.

The Research Regulatory Administrator provides regulatory, monitoring, policy development, contractual and administrative oversight for all oncology and system related research. Provides direction for the operation of the Clinical Research Trials Office, including guiding the staff in addressing priorities and workload guidelines.

Sanford Health seeks a bilingual (English/Spanish) Clinical Research Coordinator for a full‑time, temporary role through May 2027. The coordinator will support clinical trial management, plan and coordinate research studies, interpret and facilitate patient communication, and may travel locally and supervise students.

Associate Clinical Research Coordinator at Sanford Health’s Oncology Clinical Trials team. The role supports oncology trials by educating patients, physicians, and staff, coordinating study procedures, managing enrollment logs, and ensuring protocol compliance.

Associate HR Partner, Clinical Research Units (CRUs) supports CPS clinics in Dallas and Madison. Provides onsite HR support, serves as primary HR contact for employees and leaders, and manages employee relations including intake, investigations, corrective actions, and performance management.

Clinical Research Specialist at ThedaCare Regional Cancer Center in Appleton, Wisconsin. Responsible for coordinating clinical studies, including patient screening, informed consent, data collection, and source document maintenance.

Clinical Research Coordinator at Lutheran Hospital supports clinical research projects, collaborating with investigators, patients, and staff to ensure safe, ethical, efficient studies. Works full-time 40 hrs/week, Monday-Friday, in La Crosse, WI. Requires bachelor’s in Clinical Research Coordination or related field, or associate with 4 years healthcare experience (2 in clinical research).

Clinical Research Nurse I at Covance in Madison, WI. Provide high‑standard care to Phase‑1 trial participants, ensuring safety, dignity, and protocol adherence. Administer investigational drugs, perform cannulation, telemetry, ECGs, and venipuncture, and document adverse events.

Covance, a leading clinical research organization, seeks a Clinical Research Nurse I to support Phase 1 trials in Madison, WI. The role involves direct patient interaction, administering investigational drugs, monitoring safety, and documenting adverse events. Candidates must hold an associate or bachelor’s nursing degree, current RN license, CPR/AED certification, and preferably ACLS.

Covance, a leading clinical research organization, seeks a Clinical Research Technician II to support Phase 1 trials in Madison, WI. The role involves direct interaction with healthy volunteers, performing vital sign measurements, venipuncture, ECG/Holter recordings, and sample collection per protocol. Technicians monitor dietary compliance, assist with room and equipment setup, and support screening procedures.

Clinical Research Nurse I at Covance supports Phase 1 trials in Madison, WI. The role involves direct interaction with healthy volunteers, administering investigational drugs, and monitoring safety and tolerability. Nurses perform vital sign checks, ECGs, venipuncture, telemetry, and holter monitoring while ensuring participant dignity and adherence to protocols.

Clinical Research Nurse position at Covance in Madison, WI. The role involves direct interaction with healthy volunteer participants, reading clinical research protocols, and providing high-standard care in a fast-paced, team-oriented environment. Responsibilities include ensuring participant safety, maintaining emergency certifications, responding to emergencies, administering investigational compounds, performing cannulation, telemetry, holters, vital signs, ECGs, and venipuncture, obtaining informed consent, and documenting adverse events.

Clinical Research Nurse II at Covance in Madison, WI provides direct patient care in Phase 1 trials, monitoring safety and pharmacokinetics of new drugs. Responsibilities include vital sign monitoring, venipuncture, ECG/Holter recording, sample collection, dietary compliance, equipment prep, and screening procedures.

The Clinical Research Coordinator I (CRC I) at Meharry Medical College is responsible for specimen collection, processing, shipping, and tracking for the T4C initiative, maintaining lab inventory and cleanliness, and ensuring compliance with biosafety guidelines, IRB, FDA, OHRP, GCP/ICH, HIPAA, and NIH policies. The CRC I independently manages study protocols, performs venipunctures, records vital signs, and assists with IRB submissions, budgeting, and financial functions under the supervision of the Lab Manager, Medical Director, and Associate Director.

The Clinical Research Coordinator I (CRC I) will be responsible for specimen collection, processing, shipping, and tracking for T4C initiative. The CRC I will be responsible for inventory and keeping the lab clean and orderly at all times.

The Clinical Research Coordinator I (CRC I) will be responsible for specimen collection, processing, shipping, and tracking for T4C initiative. The CRC I will be responsible for inventory and keeping the lab clean and orderly at all times.