Senior Oncology Clinical Research Coordinator (Hybrid)

Actalent; False Pass (AK); Hybride; USD 41 000 - 48 000; Plein temps

Avantages offerts par ce poste

Medical, dental & vision

401(k) Retirement Plan

Life Insurance

Short/long-term disability

HSA

Résumé du poste

Actalent in Philadelphia, PA is seeking a Senior Clinical Research Coordinator to support oncology trials and direct patient interactions in a hybrid, contract-to-hire role. You will oversee multiple studies, ensure regulatory compliance, and mentor staff within a collaborative team environment.

The ideal candidate has at least two years of clinical research experience, exposure to oncology or complex drug studies, and strong skills in patient recruitment and trial management, with a Bachelor’s

Qualifications

• Minimum of two years of clinical research experience.
• Experience in oncology or complex drug studies required.
• Proficiency in patient recruitment and clinical trial management.
• Strong project management skills.

Responsabilités

• Conduct and oversee multiple clinical trials, ensuring compliance with regulatory requirements and study protocols.
• Engage directly with patients, providing support and information throughout the trial process.
• Collaborate with the Program Manager and other team members to ensure the smooth execution of clinical studies.
• Utilize and manage clinical research systems effectively.
• Mentor and train incoming staff members, fostering a collaborative and knowledgeable team environment.

Connaissances

Clinical research

Oncology

Patient recruitment

Project management

Regulatory compliance

Formation

Bachelor’s degree + 5 years

Master’s degree + 3 years

Outils

Clinical research systems

Description du poste

Actalent in Philadelphia, PA is seeking a Senior Clinical Research Coordinator to support oncology trials and direct patient interactions in a hybrid, contract-to-hire role. You will oversee multiple studies, ensure regulatory compliance, and mentor staff within a collaborative team environment.

The ideal candidate has at least two years of clinical research experience, exposure to oncology or complex drug studies, and strong skills in patient recruitment and trial management, with a Bachelor’s