Top 2706 Crc Jobs | SimplyHired

Assistant CRC
University of California San Francisco —San Francisco, CA
- Full-time
- HIPAA
- Windows
- High school diploma or GED
Telehealth Medical Coder – CRC Required - Remote
CareTalk Health —Remote
- $30 an hour
- Full-time
- Remote
- Background check
- Clinic experience
- Mid-level
Quick Apply
Clinical Research Coordinator (CRC) I
Pharmaron —Baltimore, MD
- Full-time
- 1 year
- Associate's degree
- Entry level
Quick Apply
CRC OHN
University of California San Francisco —San Francisco, CA
- Full-time
- Writing skills
- HIPAA
- Mid-level
HCC Medical Coder
vArida-Tech —Remote
- $10 - $11 an hour
- Contract
- Remote
- HIPAA
- Mid-level
Quick Apply
Consultant – Clinical Documentation Integrity (CDI) – Healthcare
Berkeley Research Group, LLC —Remote
- $90,000 - $135,000 a year
- Full-time
- Remote
- Classroom
- Nursing
- Microsoft Outlook
CRC I
Minneapolis Heart Institute Foundation —Minneapolis, MN
- $55,000 - $65,000 a year
- Microsoft Outlook
- Hospital
- BLS Certification
- Health savings account
- Paid holidays
Quick Apply
9d
Senior Clinical Trial Manager
Aveera Medical —Remote
- $125,000 - $175,000 a year
- Full-time
- Remote
- 7 years
- Organizational skills
- Senior level
- Health insurance
- Dental insurance
Quick Apply
Research Assistant
CenExel IResearch LLC —Decatur, GA
- $20 - $21 an hour
- Psychiatry
- Office
- Neurology
- Health insurance
- Dental insurance
Quick Apply
Clinical Research Coordinator I - VESPER
Henry M. Jackson Foundation —Washington, DC
- $52,800 - $57,164 a year
- Full-time
- Hybrid work
- Entry level
- Health insurance
- Dental insurance
Clinical Research Coordinator I (Long Beach)
Irvine Clinical Research —Long Beach, CA
- $25 an hour
- Full-time
- Nursing
- Psychiatry
- English
- Dental insurance
- Paid time off
Quick Apply
Children's Residential Center Therapist
Christian Children's Home of Ohio —Wooster, OH
- Full-time
- Writing skills
- LPC
- Mid-level
Quick Apply
11d
Principal Clinical Research Analyst - Class III Medical Devices (EU MDR Clinical Affairs Expert)
BIOTRONIK —Tustin, CA
- $165,000 - $185,000 a year
- Online Application
- Hybrid work
- 7 years
- Office
- Bachelor's degree
- Health savings account
- Health insurance
11h
Physician 3-Gender Affirming Care- CE69-HQ
State of Washington Dept. of Corrections —Tumwater, WA
- $208,704 - $280,752 a year
- 8 hour shift
- Background check
- Medicine
- Current TB test
- Paid holidays
- Health insurance
Vocational Rehabilitation Specialist/Case Manager
Hoover Rehabilitation Services, Inc. —Mechanicsburg, PA
- Full-time
- LPC
- Mid-level
- Master's degree
- Travel reimbursement
- Health insurance
Quick Apply
Clinical Trials Coordinator (1-2 years of experience)
Clinical Trials of South Carolina —Charleston, SC
- Full-time
- Mid-level
- Bachelor's degree
- Neurology
- Health insurance
- Dental insurance
Quick Apply
Certified Vocational Rehab Counseling Supervisor
The Fedcap Group —New York, NY
- $65,000 - $70,000 a year
- Full-time
- Addiction Medicine
- Experience working with individuals with disabilities
- Mid-level
- Paid training
- 403(b) matching
Quick Apply
Vocational Rehabilitation Specialist/Case Manager
Hoover Rehabilitation Services, Inc. —Pittsburgh, PA
- Full-time
- LPC
- Mid-level
- Master's degree
- Travel reimbursement
- Health insurance
Quick Apply
CART services - Independent Contractor needed
CIS Interpreters —Los Angeles, CA
- $100 an hour
- Night shift
- Research
- Mid-level
- US work authorization
- Flexible schedule
Quick Apply
Experienced Clinical Research Coordinator
Proscience Research Group —Culver City, CA
- $25 - $34 an hour
- Full-time
- Spanish
- Microsoft Excel
- Vital signs
- Health insurance
- 401(k)
Quick Apply
11d

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Assistant CRC

University of California San Francisco -
San Francisco, CA

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Job Details

Full-time

Qualifications

Spreadsheets
Word embeddings
Windows
High school diploma or GED
Patient interaction
Productivity software

Full Job Description

The Assistant Clinical Research Coordinator will assist the PI with clinical research coordination of the following studies:

(1) a pediatric headache study sponsored by PCORI. UCSF is identified as an enrolling site. Under the PI and Clinical Research Manager; the incumbent may coordinate the data collection and operations of this trial (REACH) Responding with Evidence and Access for Childhood and Headaches under the guidelines of the Code of Federal Regulations, Good Clinical Practice, and UCSF policies.

(2) a pediatric headache study sponsored by Pfizer. Under the PI and Clinical Research Manager; the incumbent may coordinate the data collection and operations of this study Empowering Children and Adolescents Undergoing Needle-based Procedures for Headache Treatment through Implementation of a “Headache Procedure Comfort Menu”: a Novel Clinical Tool under the guidelines of the Code of Federal Regulations, Good Clinical Practice, and UCSF policies.

The incumbent’s duties may include, but will not be limited to supporting the management and coordinating the tasks of single or multiple clinical research studies of varied size and complexity; help in research administration; assist with patient recruitment; help manage patient study source documents; perform data entry to study Case Report Form databases; collect, process and ship study specimens in accordance with study protocols; assist the PI with intermediary services and departments while overseeing data and specimen coordination; report study progress to the PI in regular team meetings; update spreadsheets tracking recruitment efforts; help coordinate subcontracts through collaborative effort with PI; assist with management of all Regulatory aspects of Investigator’s protocols in IRIS, the Committee on Human Research online system, including renewals and modifications of study protocols and the implementation of new studies; ensure study data integrity; assist with implementation of quality control procedures; participate in any internal and external audits or reviews of study protocols; and perform other duties as assigned as appropriate.

Required Qualifications:

HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities.
Excellent verbal and written communications and presentation skills ; excellent organizational skills; and excellent interpersonal skills to work effectively in a diverse team.
Proficiency with Microsoft Word, PowerPoint, and Windows.
Excellent analytical and problem-solving skills.
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.

Required Licenses and/or Certifications:

N/A

Preferred Qualifications:

Fluency in the usage of Committee of Human Research (CHR) online iIRISsystem for submission, renewal, and modification of protocols through this system.
Understanding of patient population to create rapport and a relationship, while also giving insight to what is realistic and appropriate for patient participation.
Ability to abstract data from medical records and transfer it to data collection forms or directly into databases.
Knowledge of UCSF and departmental policies for dealing with reimbursement, guidelines for research, confidentiality and HIPPA regulations, following the UCSF mission statement and purpose for research, and a clear understanding of policies and procedures on patient safety and confidentiality (electronic and hard copy medical records, patient charts, communication, etc.); knowledge of medical terminology, research policies and guidelines, guidelines for packing/shipping infectious substances, Experience with electronic Clinical Research Form databases
Experience applying the following regulations and guidelines: Good Clinical Practice Guidelines, Health Information and Accountability Act (HIPAA), The Protection of Human Research Subjects, CHR regulations for recruitment and consent of research subjects, Effective Cash Handling Procedures, Environmental Health and Safety Training and Fire Safety Training
Experience in clinical trials. Experience with protocol compliance and patient safety for Investigational Medicinal Products (IMPs).
Experience administering the Columbia Suicide Severity Rating scale (CSS-R).

About UCSF

The University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences and health professions, and excellence in patient care. It is the only campus in the 10-campus UC system dedicated exclusively to the health sciences. We bring together the world’s leading experts in nearly every area of health. We are home to five Nobel laureates who have advanced the understanding of cancer, neurodegenerative diseases, aging and stem cells.

Pride Values

UCSF is a diverse community made of people with many skills and talents. We seek candidates whose work experience or community service has prepared them to contribute to our commitment to professionalism, respect, integrity, diversity and excellence – also known as our 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 here .

Join us to find a rewarding career contributing to improving healthcare worldwide.

Equal Employment Opportunity

The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected status under state or federal law.

Salary Information

The final salary and offer components are subject to additional approvals based on UC policy.

Your placement within the salary range is dependent on a number of factors including your work experience and internal equity within this position classification at UCSF. For positions that are represented by a labor union, placement within the salary range will be guided by the rules in the collective bargaining agreement.

To learn more about the benefits of working at UCSF, including total compensation, please visit: https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html

Apply Now

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