Oncology Clinical Trials Specialist

Actalent; New Brunswick (NJ); In loco; USD 48.000 - 52.000; Tempo pieno

Vantaggi offerti da questo lavoro

Medical, dental & vision

401(k) plan

Onsite work environment

Descrizione del lavoro

Actalent is seeking a Clinical Trial Specialist to support end-to-end oncology trial activities from protocol activation through patient enrollment and data capture. The role collaborates with research nurses, physicians, and sponsors to ensure compliant conduct under GCP guidelines.

The candidate will manage study tools, consent documentation, adverse event reporting, and sponsor communications while maintaining rigorous trial records across centers in New Jersey.

Competenze

• Bachelor's degree required.
• 1–3 years of clinical research experience, preferably as a Clinical Research Coordinator.
• Experience in oncology clinical research and familiarity with tumour study groups.
• Informed consent processes and IRB/ethics documentation experience.

Mansioni

• Coordinate initiation and activation of new clinical trial protocols with required regulatory approvals.
• Prepare and organize study tools and materials for efficient trial conduct.
• Use trials management software and MS Office to maintain study tools and data.
• Review patient charts and histories to confirm protocol eligibility and collect source documents.
• Ensure IRB-approved informed consent forms are properly obtained and filed.

Conoscenze

Oncology clinical research

Informed consent

Recruitment & enrollment

Data tracking & reporting

Communication with patients

GCP & regulatory compliance

Attention to detail

Organizational skills

Formazione

Bachelors degree

Strumenti

Excel

Word

Access

Descrizione del lavoro

Actalent is seeking a Clinical Trial Specialist to support end-to-end oncology trial activities from protocol activation through patient enrollment and data capture. The role collaborates with research nurses, physicians, and sponsors to ensure compliant conduct under GCP guidelines.

The candidate will manage study tools, consent documentation, adverse event reporting, and sponsor communications while maintaining rigorous trial records across centers in New Jersey.