Oncology Clinical Research Coordinator – Multi-Trial Lead

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

Benefits offered by this job

Medical, dental & vision

401(k) retirement plan

Pre-tax and Roth post-tax benefits

Life Insurance

Short/long-term disability

Health Spending Account (HSA)

Transportation benefits

Time Off / PTO

Job summary

Actalent in the United States seeks a Clinical Research Coordinator to oversee oncology studies under the Research Director. You will coordinate subject screening, assess patients, manage data entry, and ensure GCP compliance across multiple trials with investigators and clinical staff.

The role requires handling regulatory documents, IRB submissions, adverse event reporting, and accurate study documentation while coordinating patient visits and data capture on-site in San Antonio, Texas.

Qualifications

• 2+ years of CRC experience.
• Experience with regulatory requirements and FDA GCP.
• Experience coordinating patient visits and study procedures.
• Ability to interpret medical histories and document vitals/ECGs.
• Strong data management and accurate documentation.

Responsibilities

• Execute, manage and coordinate clinical research protocols per regulatory requirements.
• Coordinate data collection and operations for several concurrent studies.
• Screen, recruit and pre-screen subjects for oncology trials.
• Oversee data and specimen collection and processing per protocol.
• Prepare and track IRB submissions and protocol renewals.

Skills

CRC experience

Clinical trial coordination

Regulatory knowledge

IRB processes

Data collection & entry

ECGs

Multi-study management

Attention to detail

Communication skills

Job description

Actalent in the United States seeks a Clinical Research Coordinator to oversee oncology studies under the Research Director. You will coordinate subject screening, assess patients, manage data entry, and ensure GCP compliance across multiple trials with investigators and clinical staff.

The role requires handling regulatory documents, IRB submissions, adverse event reporting, and accurate study documentation while coordinating patient visits and data capture on-site in San Antonio, Texas.