Top 251 Clinical research associate Jobs in Alameda Ca

Hybrid Clinical Research Coordinator
TEKBERRY —Stanford, CA
- $38 - $44 an hour
- Day shift
- Mid-level
- Data entry
- Organizational skills
- Health insurance
- Dental insurance
Quick Apply
13d
Clinical Research Coordinator 2
TEKBERRY —Stanford, CA
- $35.00 - $38.10 an hour
- Full-time
- Mid-level
- Databases
- Bachelor's degree
- Health insurance
- Dental insurance
Quick Apply
11d
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
3d
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
6d
Clinical Research Associate I (Start Up Focus)
Abbott Laboratories —Alameda, CA
- $73,900 - $116,000 a year
- Full-time
- Bachelor of Science
- Mid-level
- Office
- Health insurance
- Tuition reimbursement
6d
Clinical Research Coordinator
University of California San Francisco —Oakland, CA
- Full-time
- Bachelor of Science
- HIPAA
- Mid-level
Assistant Clinical Research Coordinator
University of California San Francisco —Oakland, CA
- Full-time
- Windows
- High school diploma or GED
- Children
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
7d
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
Research Assistant/Research Associate
Frontage Laboratories —Hayward, CA
- $62,400 - $80,000 a year
- Full-time
- Bachelor of Science
- Maintenance
- Bachelor's degree
- Disability insurance
- Health insurance
Quick Apply
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
Limited Appointment Senior Clinical Research Coordinator
University of California San Francisco —Oakland, CA
- Full-time
- Microsoft Access
- Analysis skills
- University
12d
Clinical Research Coordinator Cardiology
University of California San Francisco —San Francisco, CA
- HIPAA
- Mid-level
- High school diploma or GED
Research Associate
Heluna Health —San Francisco, CA
- $38.03 an hour
- Weekends as needed
- Spanish
- Microsoft Access
- English
Senior Clinical Research Associate (level dependent on experience)
CTI Clinical Trial Services, Inc —San Francisco, CA
- Hybrid work
- Nursing
- Mid-level
- Master's degree
- Paid parental leave
- Tuition reimbursement
Quick Apply
Staff Research Associate
University of California San Francisco —San Francisco, CA
- Full-time
- HIPAA
- Mid-level
- High school diploma or GED
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
Senior Research Associate
Onyx Bio —Berkeley, CA
- $100,000 - $130,000 a year
- Full-time
- Bachelor of Science
- Mid-level
- 3 years
- Dental insurance
- Paid time off
Quick Apply
Clinical Research Coordinator Associate
Stanford University —Stanford, CA
- $34.56 - $40.30 an hour
- Full-time
- Hybrid work
- HIPAA
- Mid-level
- University
12d

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Hybrid Clinical Research Coordinator

TEKBERRY -
Stanford, CA

Quick Apply

Job Details

$38 - $44 an hour
13 days ago

Benefits

Health insurance
Dental insurance
401(k)

Qualifications

Electronic health records (EHR) management
Research project coordination
Collaborative research
Clinical data entry
Data entry
Productivity software
Managing patient records
Medical terminology

Full Job Description

Hybrid Clinical Research Coordinator

Pay Rate Range: $38.00 - $44.00/hr. (W2) (DOE)

Duration: Approximately 6 months, afterwards there is the potential for Extension/Conversion
Schedule: Monday Friday, Day Shift, Hybrid (3 4 days onsite per week)
Location: Palo Alto, CA
Job Code: JPC-12432

Position Overview

Tekberry is seeking a detail-oriented and organized Clinical Research Coordinator to support clinical research studies within a leading academic medical environment. This role coordinates moderately complex clinical research studies from study start-up through closeout while working under the direction of the Principal Investigator and study leadership.

The ideal candidate will have previous clinical research assistant or coordinator experience, strong data management skills, and experience working with electronic medical records (EPIC preferred). This position is ideal for someone who thrives in a collaborative research environment and is passionate about supporting clinical studies that improve patient care and advance medical research.

As a Tekberry W2 employee, you will have access to health benefits including medical, dental, vision, and 401(k) options.

Responsibilities

Clinical Study Coordination

Coordinate assigned clinical research studies from study start-up through closeout.
Serve as the primary point of contact for research participants, sponsors, and regulatory agencies.
Screen, determine participant eligibility, and obtain informed consent according to study protocols.
Assist with participant recruitment strategies and enrollment activities.
Coordinate study visits, scheduling, and participant communications.
Assemble study kits and prepare materials for research visits.
Coordinate collection, processing, and documentation of study specimens.

Data Collection & Study Documentation

Collect, manage, and maintain patient and laboratory data for clinical research studies.
Complete and maintain case report forms (CRFs), flow sheets, study logs, and research databases.
Develop and maintain study documentation and tracking systems.
Ensure research data is complete, accurate, and entered according to protocol requirements.
Maintain essential study documentation in accordance with institutional and regulatory requirements.

Regulatory Compliance

Ensure compliance with study protocols, institutional policies, Good Clinical Practice (GCP), and regulatory requirements.
Prepare regulatory submissions and assist with Institutional Review Board (IRB) applications, renewals, and amendments.
Review and audit case report forms against source documentation for completeness and accuracy.
Participate in sponsor monitoring visits and regulatory audits.
Coordinate study documentation required for monitoring visits and study closeout activities.

Financial & Administrative Support

Monitor study expenditures and assist with study budget tracking.
Coordinate research billing activities and resolve billing issues with finance and management teams.
Track study procedures and research-related charges.
Support study meetings and collaborate closely with investigators, sponsors, and research staff.
Maintain organized research files and assist with additional study-related administrative tasks as assigned.

Required Qualifications

Education & Experience

Associate degree (two-year college program) with two years of related clinical research experience, or
Bachelor's degree in a related field, or
An equivalent combination of education, training, and relevant experience.
Minimum of 1 year of clinical research experience supporting clinical studies.

Required Skills

Experience coordinating or supporting clinical research studies.
Experience with clinical data entry and study documentation.
Experience working with electronic medical records (EPIC preferred).
Knowledge of medical terminology.
Strong interpersonal and communication skills.
Excellent organizational skills and attention to detail.
Ability to manage multiple priorities in a fast-paced research environment.
Proficiency with Microsoft Office Suite.
Ability to work independently while collaborating effectively with multidisciplinary teams.

Preferred Qualifications

Experience coordinating clinical research studies from start-up through closeout.
Experience preparing regulatory submissions and maintaining regulatory binders.
Experience managing study databases, case report forms, and research documentation.
Experience coordinating participant recruitment and informed consent.
Experience participating in sponsor monitoring visits and regulatory audits.
Current certification through:
- Society of Clinical Research Associates (SoCRA), or
- Association of Clinical Research Professionals (ACRP).

Top Priorities for Success

Clinical research assistant or coordinator experience.
Strong clinical data entry and documentation skills.
Experience working with electronic medical records (EPIC strongly preferred).
Excellent organizational skills and attention to detail.
Ability to coordinate multiple research activities while maintaining protocol compliance.

We need hard-working, reliable employees. If you're ready to support meaningful clinical research while helping advance patient care and medical innovation, we want to hear from you!

Tekberry is an equal opportunity employer. All qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status. Tekberry is a certified Minority Business Enterprise (MBE) and Disadvantaged Business Enterprise (DBE).

By applying to this position, you agree to receive text message updates from Tekberry regarding your application status. Msg & data rates may apply. Reply STOP to opt out.

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Refine Your Search

clinical research associate jobs in alameda ca

Hybrid Clinical Research Coordinator

Clinical Research Coordinator 2

Clinical Research, Associate I

Clinical Research Associate II

Clinical Research Associate I (Start Up Focus)

Clinical Research Coordinator

Assistant Clinical Research Coordinator

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

Clinical Research Associate

Research Assistant/Research Associate

Clinical Research Associate II

Senior Clinical Research Associate

Limited Appointment Senior Clinical Research Coordinator

Clinical Research Coordinator Cardiology

Research Associate

Senior Clinical Research Associate (level dependent on experience)

Staff Research Associate

Sr. Clinical Research Associate

Senior Research Associate

Clinical Research Coordinator Associate

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