Oncology Clinical Trials Coordinator II

Actalent; Atlanta (GA); On-site; USD 41,000 - 48,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan

Life Insurance

Short/long-term disability

HSA

PTO / Vacation

Job summary

Actalent is seeking a Clinical Research Coordinator II for an onsite role in Atlanta, GA. The candidate will coordinate oncology-focused therapeutic and interventional trials from activation to closeout, screen and enroll participants, and ensure high-quality documentation throughout the trial lifecycle.

The role emphasizes patient safety, AE/SAE reporting, and adherence to GCP guidelines while collaborating with investigators, research nurses, and multidisciplinary teams.

Qualifications

• Experience coordinating or supporting clinical trials including patient visits and follow-up.
• Knowledge of AE/SAE reporting processes and regulatory requirements.
• Familiarity with GCP guidelines and clinical trial operations.

Responsibilities

• Coordinate and manage trials from activation through closeout.
• Screen, enroll, and follow participants per protocol.
• Schedule visits and procedures for timely protocol execution.
• Maintain accurate study documentation and source data.
• Monitor patient safety and report adverse events.
• Ensure compliance with study protocols and policies.

Skills

Clinical trial operations

Participant recruitment

AE/SAE reporting

GCP guidelines

Oncology experience

Protocol adherence

Investigator collaboration

Documentation accuracy

Team collaboration

Attention to detail

Education

High school diploma with 5 years clinical trials experience

2-year degree with 2 years clinical trials experience

Bachelor's degree with 1 year clinical trials experience

Job description

Actalent is seeking a Clinical Research Coordinator II for an onsite role in Atlanta, GA. The candidate will coordinate oncology-focused therapeutic and interventional trials from activation to closeout, screen and enroll participants, and ensure high-quality documentation throughout the trial lifecycle.

The role emphasizes patient safety, AE/SAE reporting, and adherence to GCP guidelines while collaborating with investigators, research nurses, and multidisciplinary teams.