Assistant Clinical Research Coordinator II

Work Location: In Office ( No Hybrid/Remote Options Available) _*SUMMARY: *_*The Assistant Clinical Research Coordinator II (ACRC II) who, under the direction and ongoing supervision of the Site Manager and the Principal Investigator, aids in the daily function of clinical research programs on required protocols.
Responsibilities include planning, organizing, and assisting with clinical trials by conducting patient recruitment, enrollment and retention.
* *ESSENTIAL DUTIES AND RESPONSIBILITIE*S include the following.
Other duties may be assigned.
1)Comply with all company policies, procedures, and conduct.
2)Strictly adhere to confidentiality and compliance standards.
3)Assist CRC team as requested to facilitate research and business needs, 4)Communicate effectively and courteously with study patients regarding study objectives and ongoing instructions.
5)Administer questionnaires and monitor participant compliance.
6)Acknowledge study patients' needs and tends to them appropriately.
7)Collect patient medical history and conditions.
8)Obtain Informed Consent.
9)Liaison with laboratories to ensure timely participant testing.
10)Collect and evaluate concomitant medication.
11)Collect and evaluate medical records for compliance.
12)Perform study procedures such as EKG, vital signs, nasal swabs, and protocol specific procedures.
13)Verify accuracy of data collected.
14) Perform administrative tasks such as ordering supplies and equipment for the study.
15) Recruit patients for clinical trials based on criteria outlined in the study protocol.
16) Develop study e-source documents to comply with study protocol.
17) Manage all required study startup documentation, training, and timelines on assigned study protocols.
18)Meet all study protocol requirements and deadlines.
*QUALIFICATION REQUIREMENTS: *To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
The requirements listed below are representative of the knowledge, skill and/or ability required.
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
*EDUCATION and EXPERIENCE:* 1)Completion of accredited healthcare certification program, required.
2)2 years experience in running research protocols, required.
3)2 years experience in FDA regulations and GCP, required.
4)2 years experience in phlebotomy and EKG, required.
5)Exceptional attention to details and organization.
6)Must possess excellent verbal and written communication skills.
7)Excellent customer service skills with internal and external stakeholders.
8)A proven ability to multi-task in a rapidly changing environment.
Benefits: * 401(k) * Dental insurance * Employee assistance program * Health insurance * Health savings account * Life insurance * Paid time off * Vision insurance Experience level: * 2 years Schedule: * Monday to Friday Experience: * FDA regulations and GCP: 3 years (Required) * Phlebotomy and EKG: 3 years (Required) * Research Protocols: 2 years (Required) * Clinical Research Coordinator: 2 years (Required) Ability to Commute: * Inglewood, CA (Required) Job Type: Full-time Pay: $19.
00 - $24.
00 per hour Benefits: * 401(k) * Dental insurance * Health insurance * Paid time off * Vision insurance Experience level: * 2 years * 3 years Schedule: * 8 hour shift * Day shift * Monday to Friday * Weekends as needed Experience: * Clinical Research Coordinator: 2 years (Required) * Clinical Research Trails: 2 years (Preferred) Ability to Commute: * Inglewood, CA (Required) Work Location: In person