Medix
Oncology Clinical Research Coordinator - 238398
Oncology Clinical Research Coordinator - 238398
Get AI-powered advice on this job and more exclusive features. Coordinate and manage clinical trials to ensure compliance with protocols, regulations, and institutional policies, supporting participant safety and study integrity. Key Responsibilities: Facilitate site initiation and sponsor-required training for clinical protocols. Dispense study medications and coordinate with pharmacy staff as needed. Process and ship lab specimens in compliance with federal regulations. Conduct informed consent processes, ensuring proper documentation and compliance. Schedule and oversee study visits, tests, and procedures per protocol requirements. Accurately collect and report data, maintaining research subject charts and source documents. Perform or coordinate clinical procedures (e.g., blood draws, ECGs) with appropriate training. Report adverse events, protocol deviations, and violations to study sponsors and IRBs. Prepare and submit regulatory documents, including IRB applications and consent forms. Support participant recruitment, screening, enrollment, and retention. Serve as a liaison between participants, investigators, sponsors, and regulatory bodies. Assist in sponsor monitoring visits and audits, resolving findings promptly. Qualifications: 2+ years as a Clinical Research Coordinator Oncology experience required BLS Certification required Knowledge of clinical research protocols, GCP, and FDA regulations. Strong organizational, communication, and multitasking skills. Experience with clinical procedures and data management preferred. Details: Pay: $35/hr-$45/hr (Dependent on background and years of experience) Hours: Monday - Friday; Normal Business Hours; Onsite 5 Days a Week Duration:Contract to Hire (1040 Hours) Seniority level
Seniority level
Mid-Senior level Employment type
Employment type
Contract Job function
Job function
Research Industries
Hospitals and Health Care and Research Services Referrals increase your chances of interviewing at Medix by 2x Inferred from the description for this job
Medical insurance Vision insurance 401(k) Get notified when a new job is posted. Sign in to set job alerts for Clinical Research Coordinator roles.
Citrus Heights, CA $55.00-$65.00 2 weeks ago Clinical Research Associate I, PER DIEM - Tan Lab
Senior In-House CRA (Remote - Continental US)
Justice Involved Re-Entry Initiative (JI) Research Specialist
LVN Clinical Intake/Admissions Coordinator (TPAC)
Clinical Regional Coordinator (Temporary Employee Pool)
Cardiovascular Nurse Clinical Coordinator
Cardiovascular Nurse Clinical Coordinator
EMS Instructor & Paramedic Clinical Coordinator (TRAINER 3)
Were unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr
Oncology Clinical Research Coordinator - 238398
Get AI-powered advice on this job and more exclusive features. Coordinate and manage clinical trials to ensure compliance with protocols, regulations, and institutional policies, supporting participant safety and study integrity. Key Responsibilities: Facilitate site initiation and sponsor-required training for clinical protocols. Dispense study medications and coordinate with pharmacy staff as needed. Process and ship lab specimens in compliance with federal regulations. Conduct informed consent processes, ensuring proper documentation and compliance. Schedule and oversee study visits, tests, and procedures per protocol requirements. Accurately collect and report data, maintaining research subject charts and source documents. Perform or coordinate clinical procedures (e.g., blood draws, ECGs) with appropriate training. Report adverse events, protocol deviations, and violations to study sponsors and IRBs. Prepare and submit regulatory documents, including IRB applications and consent forms. Support participant recruitment, screening, enrollment, and retention. Serve as a liaison between participants, investigators, sponsors, and regulatory bodies. Assist in sponsor monitoring visits and audits, resolving findings promptly. Qualifications: 2+ years as a Clinical Research Coordinator Oncology experience required BLS Certification required Knowledge of clinical research protocols, GCP, and FDA regulations. Strong organizational, communication, and multitasking skills. Experience with clinical procedures and data management preferred. Details: Pay: $35/hr-$45/hr (Dependent on background and years of experience) Hours: Monday - Friday; Normal Business Hours; Onsite 5 Days a Week Duration:Contract to Hire (1040 Hours) Seniority level
Seniority level
Mid-Senior level Employment type
Employment type
Contract Job function
Job function
Research Industries
Hospitals and Health Care and Research Services Referrals increase your chances of interviewing at Medix by 2x Inferred from the description for this job
Medical insurance Vision insurance 401(k) Get notified when a new job is posted. Sign in to set job alerts for Clinical Research Coordinator roles.
Citrus Heights, CA $55.00-$65.00 2 weeks ago Clinical Research Associate I, PER DIEM - Tan Lab
Senior In-House CRA (Remote - Continental US)
Justice Involved Re-Entry Initiative (JI) Research Specialist
LVN Clinical Intake/Admissions Coordinator (TPAC)
Clinical Regional Coordinator (Temporary Employee Pool)
Cardiovascular Nurse Clinical Coordinator
Cardiovascular Nurse Clinical Coordinator
EMS Instructor & Paramedic Clinical Coordinator (TRAINER 3)
Were unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI. #J-18808-Ljbffr