Top 33 Clinical research coordinator associate Jobs in Sunnyvale, Ca

Clinical Research Coordinator Associate
Stanford University —Stanford, CA
- Full-time
- Hybrid work
- Patient monitoring
- HIPAA
- Mid-level
9d
Cancer Clinical Research Coordinator Associate – GI (OnSite)
Stanford University —Stanford, CA
- Full-time
- Hybrid work
- Databases
- Associate's degree
- Medical terminology
7d
Cancer Clinical Research Coordinator Associate – Head and Neck Oncology (Hybrid)
Stanford University —Stanford, CA
- $34.56 - $40.30 an hour
- Full-time
- Hybrid work
- Mid-level
- Databases
- Associate's degree
11d
Clinical Research Coordinator Associate (12-Month Fixed-Term)
Stanford University —Stanford, CA
- Full-time
- Hospital
- Inpatient
- Mid-level
Clinical Research Coordinator Associate (Two Vacancies)
Stanford University —Stanford, CA
- Full-time
- Computer literacy
- Adults
- English
9d
Clinical Research Coordinator Associate (24-Month Fixed-Term)
Stanford University —Stanford, CA
- $34.56 - $40.30 an hour
- Full-time
- Inventory management
- HIPAA
- Mid-level
Temp to Permanent Entry-Level Data Manager/Clinical Research Coordinator Associate
Stanford University Department of Bioengineering —Stanford, CA
- $35 - $38 an hour
- Temporary
- Bachelor of Science
- HIPAA
- University
Quick Apply
11d
Clinical Research Associate II
Imperative Care —Campbell, CA
- $101,000 - $106,000 a year
- Full-time
- Mid-level
- Office
- Bachelor's degree
- Health insurance
- 401(k)
Clinical Research Associate II
Corcept Therapeutics —Redwood City, CA
- $129,400 - $152,300 a year
- Bachelor of Science
- Mid-level
- 3 years
Quick Apply
On-site Clinical Research Associate
Protagonist Therapeutics —Newark, CA
- $125,000 - $135,000 a year
- English
- Mid-level
- Bachelor's degree
Quick Apply
3d
Clinical Research Associate (US-based, East Coast)
CCS Associates —San Jose, CA
- Bachelor of Science
- Writing skills
- Mid-level
Clinical Research Associate (US-based, West Coast)
CCS Associates —San Jose, CA
- Bachelor of Science
- Writing skills
- Mid-level
Senior Clinical Research Associate
Protagonist Therapeutics —Newark, CA
- $135,000 - $150,000 a year
- English
- Bachelor's degree
- Continuous improvement
Quick Apply
Associate Clinical Education Coordinator
Guardant Health —Redwood City, CA
- $57,205 - $92,550 a year
- Email
- Hybrid work
- Background check
- Mid-level
- Office
Senior Clinical Research Associate
Natera —San Carlos, CA
- $99,400 - $124,200 a year
- Bachelor of Science
- HIPAA
- Analysis skills
- Commuter assistance
- Health insurance
3d

Related jobs to explore

Based on your search for clinical research coordinator associate

Clinical Research Coordinator Associate
Stanford University —Stanford, CA
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…
5d
Temp to Permanent Entry-Level Data Manager/Clinical Research Coordinator Associate
Stanford University Department of Bioengineering —Stanford, CA
Maintain forms and documents, including consent forms and master subject logs, filing correspondence. Review medical records and/or perform telephone or in-…
$35 - $38 an hour
Quick Apply
11d

I want to receive the latest job alert for clinical research coordinator associate in sunnyvale, ca

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

clinical research coordinator associate jobs near sunnyvale, ca

Clinical Research Coordinator Associate jobs in Stanford, CA

Clinical Research Associate jobs in San Jose, CA

Clinical Research Associate jobs in Newark, CA

Clinical Research Associate jobs in Redwood City, CA

Associate Of Science Degree jobs in Denver, CO

Qualitative Research jobs in Boston, MA

Clinical Research Nurse jobs in San Antonio, TX

Clinical Research Coordinator Associate jobs in Tampa, FL

Clinical Research Coordinator Associate jobs in Phoenix, AZ

Clinical Research Coordinator Associate jobs in San Francisco, CA

Clinical Research Coordinator jobs in Connecticut

Clinical Research Coordinator Associate jobs in Hartford, CT

Event Coordinator jobs in Wichita, KS

Patient Care Coordinator jobs in Chicago, IL

Clinical Research Coordinator Associate jobs in Brighton, MI

Associate Marriage Family Therapist jobs in Los Angeles, CA

Clinical Research Coordinator Associate jobs in Atlanta, GA

Mental Health Associate No Experience jobs in New Jersey

Clinical Research Associate jobs in Portland, OR

Licensed Clinical Social Worker jobs in Torrance, CA

Clinical Research Coordinator Associate

Stanford University -
Stanford, CA

Apply Now

Job Details

Full-time
9 days ago

Qualifications

Managing scientific research projects
Managing healthcare project budgets
Process audits
Informed consent
Patient monitoring
Project documentation
Adverse event reporting
Clinical incident reports
HIPAA
Filing
Data reporting
Mid-level
Patient safety
Databases
Medical scheduling
Clinical audit and monitoring
Data management
Blood sample handling
Project monitoring
Medication supplies
Adverse drug reaction monitoring
Informed consent procedures implementation
Desktop applications
Health information regulatory compliance
Research compliance clinical trial records management
Clinical trial patient safety management
Implementing research protocols
Regulatory submission editing and review
Patient recruitment
CCRP

Full Job Description

The Clinical Research Coordinator Associate is responsible for the overall management and implementation of an assigned set of multiple research protocols assuring efficiency and regulatory compliance. These studies will be conducted at the Stanford Hospital and Clinics. He/she will work as part of a clinical trials research team and report to various Principal Investigators conducting clinical research. Responsibilities include preparation of initial study documents for IRB submission in compliance with all local, state and federal regulations; advise the IRB of amendment changes to the protocol and complete annual protocol renewals. Recruit, screen, assist in the informed consent process and enroll subjects in accordance with good clinical practice guidelines. Collect, record and maintain complete data files using good clinical practice in accordance to HIPAA regulations. He/she participates in data retrieval, reporting, and preparation of files and Case Report Forms for the various studies. The successful candidate will interact with subjects by scheduling diagnostic and research evaluation visits, perform study related assessments including collection of blood samples, processing and shipment. Maintain drug accountability, adequate study supplies and equipment. The coordinator will oversee subject compliance to the study protocol, obtain information from the study subject regarding any changes in their medications or adverse events and promptly report the findings to physicians for documentation in the subject’s medical record. Report all serious adverse events promptly to investigators, sponsors and the IRB. Protect the rights, safety and well-being of human subjects involved in the clinical trials.

PHYSICAL REQUIREMENTS*:

Frequently stand, walk, twist, bend, stoop, squat and use fine light/fine grasping.
Occasionally sit, reach above shoulders, perform desk based computer tasks, use a telephone and write by hand, lift, carry, push, and pull objects that weigh up to 40 pounds.
Rarely kneel, crawl, climb ladders, grasp forcefully, sort and file paperwork or parts, rarely lift, carry, push, and pull objects that weigh 40 pounds or more.

* - Consistent with its obligations under the law, the University will provide reasonable accommodation to any employee with a disability who requires accommodation to perform the essential functions of his or her job.

WORKING CONDITIONS:
Occasional evening and weekend hours.

WORK STANDARDS:

Interpersonal Skills: Demonstrates the ability to work well with Stanford colleagues and clients and with external organizations.
Promote Culture of Safety: Demonstrates commitment to personal responsibility and value for safety; communicates safety concerns; uses and promotes safe behaviors based on training and lessons learned.
Subject to and expected to comply with all applicable University policies and procedures, including but not limited to the personnel policies and other policies found in the University's Administrative Guide, http://adminguide.stanford.edu .

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.

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.

Certificates and Licenses Required

Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred.

Apply Now

Refine Your Search

clinical research coordinator associate jobs in sunnyvale, ca

Clinical Research Coordinator Associate

Cancer Clinical Research Coordinator Associate – GI (OnSite)

Cancer Clinical Research Coordinator Associate – Head and Neck Oncology (Hybrid)

Clinical Research Coordinator Associate (12-Month Fixed-Term)

Clinical Research Coordinator Associate (Two Vacancies)

Clinical Research Coordinator Associate (24-Month Fixed-Term)

Temp to Permanent Entry-Level Data Manager/Clinical Research Coordinator Associate

Clinical Research Associate II

Clinical Research Associate II

On-site Clinical Research Associate

Clinical Research Associate (US-based, East Coast)

Clinical Research Associate (US-based, West Coast)

Senior Clinical Research Associate

Associate Clinical Education Coordinator

Senior Clinical Research Associate

Related jobs to explore

I want to receive the latest job alert for clinical research coordinator associate in sunnyvale, ca

Explore jobs in more locations

Job Seeker Tools

Employer Tools

Browse

Stay Connected