Top 27 Clinical research coordinator associate Jobs in Stanford Ca

Clinical Research Coordinator Associate
Stanford University —Stanford, CA
- $34.56 - $40.30 an hour
- Full-time
- Hybrid work
- Inventory management
- HIPAA
- Mid-level
14d
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
5h
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
14d
Cancer Clinical Research Coordinator Associate – Hematology (Hybrid)
Stanford University —Stanford, CA
- Full-time
- Hybrid work
- Mid-level
- Databases
- Administrative experience
1d
Clinical Research Coordinator Associate (18 Month Fixed Term)
Stanford University —Stanford, CA
- $34.56 - $40.30 an hour
- Full-time
- Mid-level
- University
- Data entry
14d
Clinical Research Associate
Veracyte —South San Francisco, CA
- $110,000 - $127,000 a year
- Email
- Bachelor of Science
- Mid-level
- Bachelor's degree
Quick Apply
Clinical Research Coordinator Associate (12-Month Fixed-Term)
Stanford University —Stanford, CA
- Full-time
- Hospital
- Inpatient
- Mid-level
8d
Clinical Research, Associate I
Abbott Laboratories —Alameda, CA
- $73,900 - $116,000 a year
- Full-time
- Bachelor of Science
- Bachelor's degree
- Communication skills
- Health insurance
- Tuition reimbursement
5d
Clinical Research Coordinator Associate (Hybrid) - Stanford School of Medicine
Stanford Vascular Surgery —Pleasanton, CA
- $32 - $36 an hour
- Temporary
- Hybrid work
- Background check
- Microsoft Excel
- Microsoft Outlook
Quick Apply
8d
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
Senior Clinical Research Associate
Protagonist Therapeutics —Newark, CA
- $135,000 - $150,000 a year
- English
- Mid-level
- Bachelor's degree
Quick Apply
Sr. Clinical Research Associate
CareDx, Inc. —Brisbane, CA
- $100,000 - $130,000 a year
- Full-time
- 5 years
- Analysis skills
- Bachelor's degree
- Commuter assistance
- Employee stock purchase plan
Associate Clinical Education Coordinator
Guardant Health —Redwood City, CA
- $57,205 - $92,550 a year
- Email
- Hybrid work
- Background check
- Mid-level
- Office
7d
Clinical Research Associate (US-based, West Coast)
CCS Associates —San Jose, CA
- Bachelor of Science
- Writing skills
- Mid-level
Clinical Research Associate (US-based, East Coast)
CCS Associates —San Jose, CA
- Bachelor of Science
- Writing skills
- Mid-level
Clinical Research Associate II
Abbott Laboratories —Alameda, CA
- $81,500 - $141,300 a year
- Full-time
- Up to 50% travel
- Bachelor of Science
- Writing skills
- Health insurance
- Tuition reimbursement
8d

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Cancer Clinical Research Coordinator Associate – Head and Neck Oncology (Hybrid)
Stanford University —Stanford, CA
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…
$34.56 - $40.30 an hour
5h
Cancer Clinical Research Coordinator 2 – Head and Neck Oncology CRG (Hybrid)
Stanford University —Stanford, CA
Bachelor’s degree in a related field and two years of experience in clinical research, or an equivalent combination of education and relevant experience.
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
14 days ago

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 coordinator associate jobs in stanford ca

Clinical Research Coordinator Associate

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

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

Cancer Clinical Research Coordinator Associate – Hematology (Hybrid)

Clinical Research Coordinator Associate (18 Month Fixed Term)

Clinical Research Associate

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

Clinical Research, Associate I

Clinical Research Coordinator Associate (Hybrid) - Stanford School of Medicine

Clinical Research Associate II

Clinical Research Associate II

Senior Clinical Research Associate

Sr. Clinical Research Associate

Associate Clinical Education Coordinator

Clinical Research Associate (US-based, West Coast)

Clinical Research Associate (US-based, East Coast)

Clinical Research Associate II

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