Job Description
Job Description
Key Details :
- 100 % ONSITE, NOT open to out of state applicants
- Phlebotomy experience highly preferred but not required
Clinical Research Coordinator (CRC)
The Clinical Research Coordinator is responsible for supporting the successful execution of assigned clinical trials in compliance with GCP and ICH guidelines, HIPAA, FDA regulations, and internal standard operating procedures (SOPs).
Key Responsibilities
Working collaboratively with the clinical research team, the CRC plays a vital role in managing day-to-day study activities. Core duties include, but are not limited to :
Screening and enrolling patients for clinical studiesObtaining informed consent from study participantsCoordinating and conducting patient follow-up visitsAccurately documenting clinical data in source chartsEntering study data into electronic data capture (EDC) systems and resolving queriesCollecting vital signs and electrocardiograms (ECGs)Performing basic lab procedures per protocol, such as :Collecting and processing blood specimensOperating a centrifugePreparing, storing, and shipping lab samplesManaging specimen accountability and courier coordinationManaging medical record requests and tracking responsesMaintaining study documentation, including logs and chart filingsOrdering and organizing study-specific suppliesScheduling study visits and confirming appointments with participantsDeveloping and updating source documentation as neededSupporting monitoring visits and addressing issues promptlyEnsuring timely review of reports and patient results by the investigatorFiling serious adverse event (SAE) and protocol deviation reports with sponsors and IRBs as requiredDocumenting and reporting adverse events and any instances of non-complianceCommunicating effectively with internal teams and external stakeholdersMaintaining accurate, complete, and timely documentation in accordance with ALCOAC principlesAssisting with study recruitment, patient enrollment, and tracking as neededUpholding the confidentiality of patient, client, and company informationCompleting other assigned duties as requiredStudy Start-Up and Meeting Support
Completing all tasks necessary for study initiation, including required training and proper documentation in the Investigator Site File (ISF)Preparing for and participating in Site Initiation Visits (SIVs) and Investigator Meetings (IMs)Setting up, training on, and maintaining technology used in study operationsWe will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable federal, state, and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance (FCIHO), Los Angeles Fair Chance Ordinance for Employers (ULAC), The San Francisco Fair Chance Ordinance (FCO), and the California Fair Chance Act (CFCA).As a job position within our Clinical Sciences division, a successful completion of a background check may be required as a condition of employment. This requirement is directly related to essential job functions including but not limited to : high-risk working environments (laboratories, clinical settings), handling hazards chemicals or lab specimens, conducting direct patient care, accessing medical and confidential records, access to prescription medication or other drugs, and job duties that can cause serious injury or death as a result of error. Due to these job duties, this position has a significant impact on the business operations and reputation, as well as the safety and well-being of individuals who may be cared for as part of the job position or who may interact with staff or clients.For California Applicants :
We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable federal, state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance (FCIHO), Los Angeles Fair Chance Ordinance for Employers (ULAC), The San Francisco Fair Chance Ordinance (FCO) , and the California Fair Chance Act (CFCA).
This position is subject to a background check based on its job duties, which may include patient care, working with vulnerable populations, access to financial and confidential information, driving, working with heavy machinery, or working in a warehouse or laboratory environment. Due to these job duties, this position has a significant impact on the business operations and reputation, as well as the safety and well-being of individuals who may be cared for as part of the job position or who may interact with staff or clients.
Company Description
Here at Medix, we are dedicated to providing workforce solutions to clients throughout multiple industries. We have been named among the Best and Brightest Companies to Work For in the Nation for two consecutive years. Medix has also been ranked as one of the fastest growing companies by Inc. Magazine.
Our commitment to our core purpose of positively impacting 20,000 lives affects not only the way we interact with our clients and talent, but also with our co-workers! The goal is lofty, but it is made attainable through the hard work and dedication of our teams and their willingness to lock arms together. Are you ready to lock arms with us?
Company Description
Here at Medix, we are dedicated to providing workforce solutions to clients throughout multiple industries. We have been named among the Best and Brightest Companies to Work For in the Nation for two consecutive years. Medix has also been ranked as one of the fastest growing companies by Inc. Magazine.\r\n\r\nOur commitment to our core purpose of positively impacting 20,000 lives affects not only the way we interact with our clients and talent, but also with our co-workers! The goal is lofty, but it is made attainable through the hard work and dedication of our teams and their willingness to lock arms together. Are you ready to lock arms with us?