Example Company
Software engineer
- Location
- San Francisco
- Type
- Full time
- Compensation
- $150k-$200k
- Posted
- 2 days ago
Join a team building useful software. Work closely with engineering and design to turn new ideas into products.
Loading job details
Clinical Research Coordinator Associate
- Posted
- 2MO AGO
About the role
One of the main goals of the Stanford Innovative Neurotherapeutics Center (SINC) is to translate biological insight into therapeutic strategies, building bridges between laboratory innovation and clinical implementation. So having someone who can lead clinical implementation is crucial to the success of the center.
The Clinical Coordinator / Clinical Research Coordinator will be responsible for all aspects pertaining to clinical studies for the new to be established Stanford Innovative Neurotherapeutics Center, or SINC. Responsibilities include conducting clinical research and working independently on progressively more complex projects/assignments. Independently manage significant and key aspects of a large study or all aspects of one or more small research studies.
This position is a 1 - year fixed term role.
DESIRED QUALIFICATIONS:
3-4 years of clinical research coordinator experience.
Bachelors or Masters degree in a related field
WORKING CONDITIONS:
Occasional evening and weekend hours.
[REMOVE STATEMENT BEFORE POSTING - KEEP LANGUAGE BELOW, IF APPLICABLE. REMOVE IF NOT APPLICABLE]
Drivers License Requirements
Must possess and maintain a valid California non-commercial Class C Driver's License.
Ability to drive day or night.
When conducting university business, must comply with the California Vehicle Code and Stanford University driving requirements.
Core Duties:
- Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start-up through closeout.
- Determine eligibility of and gather consent from study participants according to protocol. Assist in developing recruitment strategies.
- Coordinate collection of study specimens and processing.
- Collect and manage patient and laboratory data for clinical research projects. Manage research project databases, develop flow sheets and other study related documents, and complete study documents/case report forms.
- Ensure compliance with research protocols, and review and audit case report forms for completion and accuracy with source documents. Prepare regulatory submissions and ensure Institutional Review Board renewals are completed.
- Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact.
- Monitor expenditures and adherence to study budgets and resolve billing issues in collaboration with finance and/or management staff.
- Interact with the principal investigator regularly, ensuring patient safety and adherence to proper study conduct.
- Ensure essential documentation and recording of patient and research data in appropriate files per institutional and regulatory requirements.
- Participate in monitor visits and regulatory audits.
Minimum Education and Experience
Two-year college degree and two years related work experience or a bachelor’s degree in a related field or an equivalent combination of related education and relevant experience.
Knowledge, Skills and Abilities:
- Strong interpersonal skills.
- Proficiency with Microsoft Office.
- Knowledge of medical terminology.
Certificates and Licenses Required
Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred.
Similar roles
Senior Research Associate, Bioanalytical & Molecular AssaysModerna
Sr. Analyst, Global Client PaymentsAvalara · Pune · Remote- S&C AssociateASME (The American Society of Mechanical Engineers) · New York · Washington, DC · Houston
Verification Authorization Associate (Hybrid)Caris Life Sciences
Senior Scientist, Discovery ScienceApriori Bio · Cambridge
Staff/Sr. Staff/Principal AI research scientistWRITER · San Francisco · New York