What are the responsibilities and job description for the Senior Clinical Research Coordinator position at Alliance Clinical Network?
JOB LOCATION/SCHEDULE: Monday – Friday / On-Site / Los Angeles
COMPANY OVERVIEW: At Alliance Clinical Network we’re people with a purpose, dedicated to advancing medical innovation and healing technology through groundbreaking research. We bring our energy and our passion to improving patient lives every day.
SUMMARY: We are seeking a Sr Clinical Research Coordinator to join ACN and lead our clinical operations team at our Los Angeles location. In this role, you’ll have the opportunity to train and support staff managing multiple studies. If you’re an enthusiastic, detail-orientated lead CRC looking for your next step – we’d like to meet you.
Essential Duties And Responsibilities
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 accommodation may be made to enable individuals with disabilities to perform the essential functions.
Education And Expreience
COMPANY OVERVIEW: At Alliance Clinical Network we’re people with a purpose, dedicated to advancing medical innovation and healing technology through groundbreaking research. We bring our energy and our passion to improving patient lives every day.
SUMMARY: We are seeking a Sr Clinical Research Coordinator to join ACN and lead our clinical operations team at our Los Angeles location. In this role, you’ll have the opportunity to train and support staff managing multiple studies. If you’re an enthusiastic, detail-orientated lead CRC looking for your next step – we’d like to meet you.
Essential Duties And Responsibilities
- Partner with Regional Site Director to ensure compliance and productivity of all clinical site staff and operations.
- Manage, train and support clinical site staff.
- Review, comprehend and communicate study protocols.
- Oversee Site Initiation Visit (SIV), Pre-Study Validation Visit (PSV) and Interim Monitoring Visit (IMV).
- Assist CRC team as requested to facilitate research and business needs.
- Conduct and manage clinical trials in accordance with the study protocol guidelines and internal SOP’s.
- Ensure all data is entered into sponsor’s data portal and all queries are resolved in a timely manner.
- Work closely with CRO/CRA and IRB.
- Perform administrative tasks such as ordering supplies and equipment for the study.
- Manage all required study start up documentation, training and timelines on assigned study protocols.
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 accommodation may be made to enable individuals with disabilities to perform the essential functions.
Education And Expreience
- Associate’s degree and/or completion of accredited healthcare certification program, required.
- Comfortable stepping into a leadership role.
- 2 years’ experience in clinical research, required.
- 2 years’ experience working as a Clinical Research Coordinator, preferred.
- Comprehensive knowledge of FDA, GCP & confidentiality.
- Exceptional attention to detail and organization.
- Excellent written and communication skills.
- A proven ability to multi-task in a rapidly changing environment.
Salary : $25 - $30