Clinical Research Site Specialist 257542

Medix™; Los Alamitos (CA); On-site; USD 95,000 - 120,000; Full time

Job summary

Medix is seeking a full-time onsite Clinical Research Site Specialist in California’s Los Alamitos area to scale site operations and reopen enrollment in the Oncology space. Travel locally may be required, and benefits begin after 30 days.

This consultant-style role focuses on SOPs, process standardization, and mentoring staff to ensure site stability and growth, transitioning from patient-facing work to study start-up and project management support.

Qualifications

• Must have extensive experience in clinical research coordination.
• Proven track record in research with ability to manage site processes and staff functions.
• Recent and relevant experience in Oncology research.

Responsibilities

• Create, implement and enforce SOPs to improve site quality and compliance.
• Scale the site by managing enrollment and addressing legacy issues.
• Mentor staff as subject matter expert to ensure full functionality.

Skills

Clinical Research Coordinator

Research management

Oncology experience

Job description

We are looking to add a full time onsite Clinical Research Site Specialist to a well established research group in the Oncology space. There will be some local travel required for this role and benefits are offered after 30 days.

Previous experience in Oncology is required- this is a great opportunity for a Coordinator who is looking to move away from patient facing work and focus on study start up/Project Management support.

Responsibilities

This is a consultant-style role focused on scaling site operations, standardizing processes, and reopening the site for enrollment. The specialist will serve as a proactive backfill to ensure site stability and growth.

• Process Optimization: Create, implement, and ensure adherence to SOPs to improve site quality and compliance.
• Site Scaling: Upscale the site by managing open enrollment and correcting legacy operational issues.
• Consultancy: Act as a subject matter expert to mentor existing staff and ensure they are fully functional.

Required Skills

• Full-fledged Clinical Research Coordinator (CRC): Must have extensive experience in clinical research coordination.
• Research & Managerial Experience: Proven track record in research with the ability to manage site processes and staff functions.
• Oncology Specialization: Recent and relevant experience in Oncology research is strictly required.