Clinical Research Coordinator – pancreatic & GI tumors Job at University of California San Francisco
The activities of the CRC include identification and consenting of patients with suitable neoplasms, attending and collecting biological samples removed during clinical procedures, organization, processing, and analysis of relevant clinical and research data, and assistance with preparation of presentations, grant applications, and publications. The CRC will also be responsible for coordinating and managing the daily activities of clinical trials active in the division.
To see the salary range for this position (we recommend that you make a note of the job code and use that to look up): TCS Non-Academic Titles Search (ucop.edu)
Please note: The compensation ranges listed online for roles not covered by a bargaining unit agreement are very wide, however a job offer will typically fall in the range of 80% - 120% of the established mid-point. An offer will take into consideration the experience of the final candidate AND the current salary level of individuals working at UCSF in a similar role.
For roles covered by a bargaining unit agreement, there will be specific rules about where a new hire would be placed on the range.
To learn more about the benefits of working at UCSF, including total compensation, please visit: https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html
Department Description
Required Qualifications
- HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities; and/or equivalent experience/training.
- Experience in clinical research or demonstrated research or training experience that translates into a clinical research setting
- Attention to detail; strong interpersonal skills; excellent, effective verbal and written communication skills to coordinate with subjects, team members, other departments and outside institutions; and the ability to multi-task in a fast-paced environment while working with a diverse subject population
- Ability to work well independently, complete projects in a timely manner, and prioritize multiple projects to ensure the completion of essential tasks by deadlines
- Ability to travel between one or more campuses via UCSF shuttle
Preferred Qualifications
- Experience in handling biospecimens
- Experience with APEX/other electronic medical records
- Experience in patient interviews, consent procedures
- Experience with data entry, analysis, and reporting
- Understanding of HIPAA and IRB approval process
- Experience with scientific presentations and manuscript preparation
- Interest in pursuing a career in a medical or medical research field
- Demonstrated knowledge and understanding of research
- Prior experience with various computer programs (Microsoft Office; internet-based databases)
- Working knowledge of, or demonstrated ability to learn federal, state, and local research regulations and guidelines, and research practice methods in a laboratory or clinical setting
- Knowledge of medical terminology, and/or the ability to apply information to the assessment, interpretation, and processing of medical data
- Ability to independently interpret and apply policies, respond to requests, resolve issues, and provide assistance to faculty and staff at all levels in a team-oriented environment
About UCSF
Pride Values
In addition to our PRIDE values, UCSF is committed to equity – both in how we deliver care as well as our workforce. We are committed to building a broadly diverse community, nurturing a culture that is welcoming and supportive, and engaging diverse ideas for the provision of culturally competent education, discovery, and patient care. Additional information about UCSF is available at diversity.ucsf.edu
Join us to find a rewarding career contributing to improving healthcare worldwide.
Equal Employment Opportunity
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