Top 266 Clinical research associate Jobs in Brisbane, Ca

Clinical Research Coordinator Associate
Stanford University —Stanford, CA
- $34.56 - $40.30 an hour
- Full-time
- Hybrid work
- Inventory management
- HIPAA
- Mid-level
Clinical Research Coordinator Associate (2 Vacancies) (On-Site)
Stanford University —Stanford, CA
- Full-time
- HIPAA
- Mid-level
- Databases
Clinical Research Coordinator
University of California San Francisco —San Francisco, CA
- Full-time
- Surgery
- Bachelor of Science
- Mid-level
Clinical Research Associate
Alameda Health System —Oakland, CA
- $49.48 - $60.16 an hour
- Hospital
- BLS Certification
- Mid-level
Quick Apply
Clinical Research Coordinator Associate (12-Month Fixed-Term)
Stanford University —Stanford, CA
- Full-time
- Hospital
- Inpatient
- Mid-level
Clinical Research, Associate II
Abbott Laboratories —Alameda, CA
- $81,500 - $141,300 a year
- Full-time
- Bachelor of Science
- Mid-level
- Bachelor's degree
- Health insurance
- Tuition reimbursement
9d
Clinical Research Coordinator Associate (1-Year Fixed-Term)
Stanford University —Stanford, CA
- Full-time
- Inpatient
- Mid-level
- Databases
11d
Assistant Clinical Research Coordinator
University of California San Francisco —San Francisco, CA
- Full-time
- Microsoft Excel
- High school diploma or GED
- University
On-site Clinical Research Associate
Protagonist Therapeutics —Newark, CA
- $125,000 - $135,000 a year
- English
- Mid-level
- Office
Quick Apply
Clinical Research Associate I
Abbott Laboratories —Alameda, CA
- $73,900 - $116,000 a year
- Full-time
- Bachelor of Science
- Mid-level
- Bachelor's degree
13d
Assistant Clinical Research Coordinator, Emergency Medicine (Hybrid Opportunity)
Stanford University —Stanford, CA
- Full-time
- Hybrid work
- Vital signs
- Addiction Medicine
- University
3d
Assistant Clinical Research Coordinator
Stanford University —Redwood City, CA
- Extended hours
- Hybrid work
- Vital signs
- Office
- Administrative experience
8d
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
Clinical Research Coordinator II – Oncology (Onsite)
VertiSystem Inc —Stanford, CA
- $44.82 - $51.72 an hour
- Contract
- HIPAA
- Mid-level
- Bachelor's degree
Quick Apply
12d
Clinical Research Coordinator
Confidential —San Carlos, CA
- $30 - $45 an hour
- Part-time
- HIPAA
- Mid-level
- In-person
- Flexible schedule
Quick Apply
4d
Clinical Research Coordinator Associate (Two Vacancies)
Stanford University —Stanford, CA
- Full-time
- Computer literacy
- Adults
- English
Clinical Research Coordinator (San Francisco)
University of California, Riverside —San Francisco, CA
- $34.37 - $55.27 an hour
- Full-time
- Microsoft Access
- Psychiatry
- Mid-level
- Free parking
- Disability insurance
Quick Apply
13d
Sr. Clinical Trial Associate
ALX Oncology Inc. —South San Francisco, CA
- $115,000 - $125,000 a year
- Full-time
- Hybrid work
- Mid-level
- Office
- 3 years
- 401(k)
Quick Apply
Staff Research Associate 1 (9613C), Helen Wills Neuroscience Institute #86040
University of California Berkeley —Berkeley, CA
- $28.69 - $29.36 an hour
- Full-time
- Mid-level
- University
- Neurology
Clinical Research Coordinator (1/2)
University of California San Francisco —San Francisco, CA
- Full-time
- Mid-level
- Windows
- High school diploma or GED
6d

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Clinical Research Coordinator Associate

Stanford University -
Stanford, CA

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Job Details

Full-time
$34.56 - $40.30 an hour

Qualifications

Productivity software
Medical terminology

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.

Duties include*:

Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out.
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.

* - Other duties may also be assigned

Qualifications:

EDUCATION & EXPERIENCE (REQUIRED):

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 (REQUIRED):

Strong interpersonal skills.
Proficiency with Microsoft Office.
Knowledge of medical terminology.

CERTIFICATIONS & LICENSES:

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

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.

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.

The expected pay range for this position is $34.56 to $40.30 per hour.

Stanford University provides pay ranges representing its good faith estimate of the salary or hourly wage the university reasonably expects to pay for a position upon hire. The pay offered to a selected candidate will be determined based on factors such as (but not limited to) the scope and responsibilities of the position, the qualifications of the selected candidate, departmental budget availability, internal equity, geographic location, and external market pay for comparable jobs.

At Stanford University, base pay represents only one aspect of the comprehensive rewards package. The Cardinal at Work website ( https://cardinalatwork.stanford.edu/benefits-rewards ) provides detailed information on Stanford's extensive range of benefits and rewards offered to employees. Specifics about the rewards package for this position may be discussed during the hiring process.

Consistent with its obligations under the law, the University will provide reasonable accommodations to applicants and employees with disabilities. Applicants requiring a reasonable accommodation for any part of the application or hiring process should contact Stanford University Human Resources by submitting a contact form .

Stanford is an equal employment opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected
by law.

The job duties listed are typical examples of work performed by positions in this job classification and are not designed to contain or be interpreted as a comprehensive inventory of all duties, tasks, and responsibilities. Specific duties and responsibilities may vary depending on department or program needs without changing the general nature and scope of the job or level of responsibility. Employees may also perform other duties as assigned.

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Refine Your Search

clinical research associate jobs in brisbane, ca

Clinical Research Coordinator Associate

Clinical Research Coordinator Associate (2 Vacancies) (On-Site)

Clinical Research Coordinator

Clinical Research Associate

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

Clinical Research, Associate II

Clinical Research Coordinator Associate (1-Year Fixed-Term)

Assistant Clinical Research Coordinator

On-site Clinical Research Associate

Clinical Research Associate I

Assistant Clinical Research Coordinator, Emergency Medicine (Hybrid Opportunity)

Assistant Clinical Research Coordinator

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

Clinical Research Coordinator II – Oncology (Onsite)

Clinical Research Coordinator

Clinical Research Coordinator Associate (Two Vacancies)

Clinical Research Coordinator (San Francisco)

Sr. Clinical Trial Associate

Staff Research Associate 1 (9613C), Helen Wills Neuroscience Institute #86040

Clinical Research Coordinator (1/2)

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