Clinical Research Nurse - 254795

Clinical Research Nurse (Oncology)

Location: Mobile, AL 36607

Therapeutic Area: Oncology

Position Type: Full-Time Contract

• Duration: 7 Months
• Schedule: Monday – Friday, 40 hours per week

Position Summary

We are seeking an experienced Clinical Research Nurse (CRN) to support an oncology clinical trial in Mobile, AL. The successful candidate will play a critical role in the coordination and execution of study activities, ensuring protocol compliance, participant safety, and high-quality data collection.

This position requires a strong clinical research background, preferably in oncology, with the ability to manage multiple study responsibilities in a fast-paced research environment.

Key Responsibilities

Clinical Trial Coordination

• Coordinate and manage daily clinical trial activities in accordance with study protocols, GCP guidelines, and regulatory requirements.
• Conduct participant screening and enrollment activities.
• Perform data entry and data verification to ensure accuracy and completeness.
• Prepare study visits and support protocol-required procedures.
• Assist with query resolution and sponsor/site communications.
• Maintain study documentation and regulatory records.

Nursing Responsibilities

• Perform non-invasive screening procedures.
• Administer study medication per protocol requirements.
• Monitor participant safety and document adverse events as appropriate.
• Provide participant education and study-related support.

Participant Management

• Conduct participant follow-up activities and retention efforts.
• Monitor and support e-Diary compliance.
• Coordinate participant scheduling and visit preparation.
• Serve as a primary point of contact for study participants.

Study Support Activities

• Provide laboratory kit support and sample management assistance.
• Support source documentation review and verification.
• Assist with protocol compliance monitoring and quality control activities.
• Collaborate with investigators, sponsors, and study team members to ensure successful study execution.

Qualifications

Required

• Clinical Research Nurse (CRN) experience.
• Experience supporting clinical trials in an oncology setting.
• Knowledge of ICH-GCP guidelines and clinical research regulations.
• Strong organizational, documentation, and communication skills.
• Ability to manage multiple priorities and meet study deadlines.

Preferred

• Oncology nursing experience.
• Experience administering study medications.
• Familiarity with electronic data capture (EDC) systems and e-Diary platforms.
• Experience with participant recruitment, retention, and follow-up activities.

Skills

• Clinical trial coordination
• Oncology research
• Data entry and verification
• Study medication administration
• Participant screening and follow-up
• E-Diary compliance management
• Query resolution
• Laboratory kit support
• Study visit preparation
• Regulatory compliance

Join a dedicated oncology research team and contribute to advancing innovative cancer treatments through the successful execution of the oncology clinical trial.