Oncology Clinical Research Coordinator (Prostate/Bladder)

Actalent; San Antonio (TX); On-site; USD 32,000 - 41,000; Full time

Benefits offered by this job

Medical, dental & vision

Critical Illness, Accident, and-Hospi

401(k) Retirement Plan

Pre-tax and Roth post-tax

Life Insurance (Voluntary Life & AD&D)

Short and long-term disability

Health Spending Account (HSA)

Transportation benefits

Employee Assistance Program

Time Off/Leave (PTO, Vacation or Sick)

Job summary

Actalent in San Antonio, TX is seeking a Clinical Research Coordinator to oversee oncology studies in prostate and bladder cancers. You will coordinate protocols, ensure data integrity, recruit subjects, and support regulatory compliance under supervision.

The role is full-time, on-site, with a typical M-F 8:00 a.m. to 5:00 p.m. schedule. Prior experience in oncology trials and adverse event documentation is preferred.

Qualifications

• Minimum 2 years as a Clinical Research Coordinator in a clinical trial setting.
• Hands-on experience with trials phases I–III and protocol requirements.
• Experience with pre-screening patients and subject recruitment.
• Document adverse events per regulatory and protocol requirements.

Responsibilities

• Execute, manage and coordinate clinical research protocols under supervision.
• Coordinate data collection and day-to-day operations across multiple studies.
• Screen/pre-screen potential participants and facilitate informed consent.

Skills

Clinical Research Coord

Trial phases I-III

Patient recruitment

Adverse event documentation

ECGs

Phlebotomy

Job description

Actalent in San Antonio, TX is seeking a Clinical Research Coordinator to oversee oncology studies in prostate and bladder cancers. You will coordinate protocols, ensure data integrity, recruit subjects, and support regulatory compliance under supervision.

The role is full-time, on-site, with a typical M-F 8:00 a.m. to 5:00 p.m. schedule. Prior experience in oncology trials and adverse event documentation is preferred.