The Clinical Research Coordinator (CRC) will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate research protocols, as directed by the Clinical Research Supervisor and/or Principal Investigator (PI).
Locations (2)
San Francisco, California, United States
Oakland, California, United States
Responsibilities
Support management and coordinate tasks of single or multiple clinical research studies
Manage and report on study results
Create, clean, update, and manage databases and comprehensive datasets and reports
Coordinate staff work schedules and assist with training of Assistant CRCs
Manage Investigator’s protocols in the Committee on Human Research online system
Requirements
High School Diploma; or equivalent experience/training
BS Degree
Nice to have: Fluency in the usage of Committee of Human Research (CHR) online iMEDris system
Nice to have: Certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals
Nice to have: Understanding of patient population to create rapport and a relationship
Support the execution of clinical trials as a Clinical Research Nurse, ensuring protocol adherence and patient care.
Responsibilities
Assisting in the planning, implementation, and coordination of clinical research activities in accordance with study protocols, regulatory guidelines, and SOPs.
Conducting patient assessments, administering study treatments, and performing clinical procedures as required by the research protocol.
Collecting, recording, and maintaining accurate and complete data documentation, including medical histories, vital signs, adverse events, and laboratory results, in eCRFs and study databases.
Collaborating with multidisciplinary teams, including investigators, study coordinators, and regulatory staff, to ensure efficient study conduct, participant recruitment, and retention.
Providing education and counseling to study participants and their families regarding study procedures, treatment regimens, and informed consent.
Supports the Data Analyst team in managing and resolving data discrepancies between clients and internal databases, ensuring compliance with GCP guidelines and quality standards.
Responsibilities
Ensure seamless communication and proactive follow-up with internal stakeholders, clients, and cross-functional teams to facilitate timely resolution of data discrepancies.
Analyze and resolve simple to moderately complex client data discrepancies, updating databases as required.
Perform data revisions ranging from basic to highly complex, adhering to established data revision and data cleaning processes.
Support Workflow Leads and Client Leads in the strategic execution of data reconciliation activities and query management processes.
Attend mandatory Data Reconciliation Center (DRC) meetings and participate in training programs related to process enhancements, system updates, and data reconciliation best practices.
Requirements
Bachelor’s degree in life science or related field
Nice to have: Bachelor’s or master’s degree in science, Life Sciences, Data Management, or related field
Nice to have: Minimum of 2 years of professional experience
Supports the Data Analyst team in managing and resolving data discrepancies between clients and internal databases, ensuring compliance with GCP and quality standards.
Responsibilities
Ensure seamless communication and proactive follow-up with internal stakeholders, clients, and cross-functional teams
Analyze and resolve client data discrepancies, updating databases as required
Perform data revisions ranging from basic to highly complex
Support Workflow Leads and Client Leads in data reconciliation activities
Attend mandatory Data Reconciliation Center meetings and training programs
Requirements
Bachelor’s degree in life science or related field
Nice to have: Bachelor’s or master’s degree in science, Life Sciences, Data Management, or related field
Nice to have: Minimum of 2 years of professional experience
Supports the Data Analyst team in managing and resolving data discrepancies between clients and internal databases, ensuring timely and accurate responses and compliance with GCP guidelines.
Responsibilities
Ensure seamless communication and proactive follow-up with internal stakeholders, clients, and cross-functional teams to facilitate timely resolution of data discrepancies.
Analyze and resolve simple to moderately complex client data discrepancies, updating databases as required.
Perform data revisions ranging from basic to highly complex, adhering to established data revision and data cleaning processes.
Support Workflow Leads and Client Leads in strategic execution of data reconciliation activities and query management processes.
Attend mandatory Data Reconciliation Center meetings and participate in training programs related to process enhancements.
Requirements
Bachelor’s degree in life science or related field
Nice to have: Bachelor’s or master’s degree in science, Life Sciences, Data Management, or related field
Nice to have: Minimum of 2 years of professional experience
Supports the Data Analyst team in managing and resolving data discrepancies between clients and internal databases, ensuring timely and accurate responses while maintaining compliance with GCP guidelines.
Responsibilities
Ensure seamless communication and proactive follow-up with internal stakeholders, clients, and cross‑functional teams
Analyze and resolve client data discrepancies, updating databases as required
Perform data revisions ranging from basic to highly complex
Support Workflow Leads and Client Leads in data reconciliation activities
Attend mandatory DRC meetings and participate in training programs
Requirements
Bachelor’s degree in life science or related field
Nice to have: Bachelor’s or master’s degree in science, Life Sciences, Data Management, or related field
Nice to have: Minimum of 2 years of professional experience
The Clinical Research Program Manager will oversee compliance and quality assurance reviews for Montefiore Einstein Cancer Clinical Trials Office, managing monitoring activities, regulatory reviews, and CAPA processes.
Compensation
$84,000.00-$105,000.00
Responsibilities
Provide compliance and quality assurance reviews for Montefiore Einstein Cancer Clinical Trials Office
Conduct ongoing monitoring activities including patient case reviews, pharmacy reviews, and regulatory reviews
Determine compliance concerns and formal actions
Provide routine reviews and determine if formal actions are warranted
Work under the direction of the Director, Quality Assurance and provide feedback on findings and evaluation of CAPA
Coordinates patient enrollment for the Mass General Brigham Biobank, educating and recruiting patients, obtaining consent, and managing data in a clinical research setting.
Compensation
$21.00 - $29.01/Hourly
Responsibilities
Educate and recruit patients from outpatient and inpatient settings
Obtain consent and explain research protocols
Enter and maintain patient and survey data
Collaborate with physicians and clinic staff to integrate recruitment into workflows
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