Clinical Research Coordinator - 253067 (Cerritos)
Medix™, Cerritos, CA, United States
We are hiring for a CRC in Cerritos to collaborate on Oncology clinical trials. This position is 100% onsite, and a contract-to-hire opportunity (opportunity to be brought on permanently based on performance and clinic needs). Pay will depend on years of experience and knowledge within Oncology clinical trials.
Position Overview:
The Clinical Research Coordinator (CRC) is responsible for the day-to-day coordination and management of clinical trials, ensuring studies are conducted in compliance with protocol requirements, regulatory guidelines, and Good Clinical Practice (GCP).
Key Responsibilities:
Coordinate and oversee clinical trial activities from study start-up through close-out
Screen, recruit, and enroll study participants in accordance with protocol criteria
Obtain informed consent and ensure patient understanding of study procedures
Schedule and conduct study visits, including collection of clinical data and source documentation
Maintain accurate and timely data entry in electronic data capture (EDC) systems
Ensure compliance with study protocols, GCP, and applicable regulatory requirements
Manage investigational product accountability, storage, and documentation as applicable
Communicate effectively with investigators, sponsors, CROs, and site staff
Prepare for and support monitoring visits, audits, and inspections
Qualifications:
Bachelor’s degree or equivalent experience in a health or science-related field preferred
Prior experience in Oncology highly preferred
Strong knowledge of GCP, ICH guidelines, and clinical trial processes
Excellent organizational, time management, and communication skills
Ability to work independently and manage multiple priorities
Medix Sick Time Policy:
You will receive
1 hour
of
sick time
for every
40 hours worked
and thereafter
**Please note that if you're in a city/state with unique Sick time requirements, the city/state's policy will override Medix's internal Sick Time policy.
You will be paid by Medix and will ONLY be paid for the hours that you work.
You will NOT be paid for any time off (appointments, vacations, holidays, etc.) unless you have unused sick time hours and have properly requested to be paid for that time off.
Benefits:
Paid Sick Leave (Medix provides paid sick leave according to state and local sick leave ordinances)
Health Benefits / Dental / Vision (Medix Offers 6 different health plans: 3 Major Medical Plans, 2 Fixed Indemnity Plans (Standard and Preferred), and 1 Minimum Essential Coverage (MEC) Plan. Eligibility for health benefits is based on verifying that an average of
30 hours per week
during the first 4 weeks of the work assignment has been met. If you meet eligibility requirements and take action to enroll, you will be covered no earlier than 60 days into your assignment, depending on plan selection(s).)
401k (eligible on the first 401k open enrollment date following 6 consecutive months on assignment. 401k Open Enrollment dates are 1/1, 4/1, 7/1, and 10/1)
Short Term Disability Insurance
Term Life Insurance Plan
Position Overview:
The Clinical Research Coordinator (CRC) is responsible for the day-to-day coordination and management of clinical trials, ensuring studies are conducted in compliance with protocol requirements, regulatory guidelines, and Good Clinical Practice (GCP).
Key Responsibilities:
Coordinate and oversee clinical trial activities from study start-up through close-out
Screen, recruit, and enroll study participants in accordance with protocol criteria
Obtain informed consent and ensure patient understanding of study procedures
Schedule and conduct study visits, including collection of clinical data and source documentation
Maintain accurate and timely data entry in electronic data capture (EDC) systems
Ensure compliance with study protocols, GCP, and applicable regulatory requirements
Manage investigational product accountability, storage, and documentation as applicable
Communicate effectively with investigators, sponsors, CROs, and site staff
Prepare for and support monitoring visits, audits, and inspections
Qualifications:
Bachelor’s degree or equivalent experience in a health or science-related field preferred
Prior experience in Oncology highly preferred
Strong knowledge of GCP, ICH guidelines, and clinical trial processes
Excellent organizational, time management, and communication skills
Ability to work independently and manage multiple priorities
Medix Sick Time Policy:
You will receive
1 hour
of
sick time
for every
40 hours worked
and thereafter
**Please note that if you're in a city/state with unique Sick time requirements, the city/state's policy will override Medix's internal Sick Time policy.
You will be paid by Medix and will ONLY be paid for the hours that you work.
You will NOT be paid for any time off (appointments, vacations, holidays, etc.) unless you have unused sick time hours and have properly requested to be paid for that time off.
Benefits:
Paid Sick Leave (Medix provides paid sick leave according to state and local sick leave ordinances)
Health Benefits / Dental / Vision (Medix Offers 6 different health plans: 3 Major Medical Plans, 2 Fixed Indemnity Plans (Standard and Preferred), and 1 Minimum Essential Coverage (MEC) Plan. Eligibility for health benefits is based on verifying that an average of
30 hours per week
during the first 4 weeks of the work assignment has been met. If you meet eligibility requirements and take action to enroll, you will be covered no earlier than 60 days into your assignment, depending on plan selection(s).)
401k (eligible on the first 401k open enrollment date following 6 consecutive months on assignment. 401k Open Enrollment dates are 1/1, 4/1, 7/1, and 10/1)
Short Term Disability Insurance
Term Life Insurance Plan