The Angeles Clinic & Research Institute has established an international reputation for developing new cancer therapies, providing the best in experimental and traditional treatments, and expertly guiding and training the next generation of clinicians. Our board-certified fellowship-trained medical oncologists, surgeons, immunotherapists, pathologists, and dermatologists work closely together to advance cancer care. We are committed to bringing innovative therapeutic options to all of our patients with cancer!

Join our team and contribute to groundbreaking research!

The Clinical Research Coordinator III (CRC Lead) is responsible for project allocation and immediate oversight of clinical research coordinators and clinical research associates, along with primary coordination of assigned studies.  This includes managing schedules and coverage for the coordinator team, improving efficiency of research systems and processes, training of personnel, and resolution of day-to-day administrative and operational problems to ensure the successful implementation of research protocols.
 
Primary Duties and Responsibilities
•    Responsible for immediate oversight of CRC team, including project allocation, staff scheduling and staff training; contributes to performance reviews for CRC team.
•    Identifies and ensures needed resources and logistics for research activities, including determining appropriate course of action in solving day-to-day research operations problems.
•    Responsible for departmental reporting related to protocol activity, accrual data, workload, and other research information; present this information to management.
•    Participates in project feasibility reviews and study initiation visits and provides strategic mentorship on study set-up and implementation.
•    Identifies quality and performance improvement opportunities and collaborates with staff in the development of action plans to improve quality and efficiency.
•    Provides oversight for institutional, pharmaceutical and internal audits, including facilitating third party study monitoring and designs and implements needed corrective actions.
•    Provides assistance with research project budget development, including identifying and classifying routine care vs. research related care and provides assistance with research participant research billing and reconciliation.
•    Provides study coordination for assigned projects, including patient screening and consenting, regulatory reporting, completion required data collection, maintenance of source documents, facilitation of all study logistics to ensure successful protocol implantation and patient safety.
•    Participate in meetings and conferences related to research activities, including research staff meetings.
•    Participate in planning, workshops, evaluation meetings, and seminars, educational or administrative meetings as vital or requested.
 

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Educational Requirements:

• Bachelor's Degree in related field required
  Master's Degree preferred
  

Licenses:

Certification In Clinical Research SoCRA or ACRP certification within1 Year
Basic Life Support (BLS) Certification needs to be the AHA Healthcare Provider Type Only Required.
Phlebotomy Certification CA Current Phlebotomy Cert from State of CA Preferred
Certified Registered Medical Assistant Preferred

Experience:

5 years Clinical research coordination or related experience required

Physical Demands:

Standing, Walking, Sitting, Lifting, Carrying, Pushing, Pulling, Stooping, Kneeling, Crouching, Reaching, Handling, Grasping, Feeling, Talking, Hearing, Repetitive Motions, Eye/Hand/Foot Coordination