Top 11 Clinical research coordinator Jobs in Lancaster, Ca

Clinical Research Sub-Investigator (NP, PA, MD, or DO)
Chemidox Clinical Trials —Lancaster, CA
- Full-time
- Spanish
- Medicine
- Management
- Paid holidays
- Health insurance
Quick Apply
6d
PMI Materials Coordinator (supporting the Air Force Research Lab)
ASRC Federal —Edwards AFB, CA
- $32 an hour
- Full-time
- High school diploma or GED
- SharePoint
- Entry level
- Paid holidays
- Health insurance
Quick Apply
Quality Clinical Safety Coordinator - Quality Mgmt/Clinical Safety - Full Time/Days - Req#2117934814
Antelope Valley Medical Center —Lancaster, CA
- $107,868.80 - $170,289.60 a year
- Full-time
- Microsoft Word
- Nursing
- Microsoft Excel
Quick Apply
Hazardous Materials Coordinator (supporting the Air Force Research Lab)
ASRC Federal —Edwards AFB, CA
- $70,905 - $106,357 a year
- Overtime
- Mid-level
- Travel
- 1 year
- Paid holidays
- Health insurance
Quick Apply
6d
Clinical Training & Skills Development Coordinator CCU - Education - Full Time/Days - Req #211796693
Antelope Valley Medical Center —Lancaster, CA
- $56.25 - $86.35 an hour
- Full-time
- Nursing
- RN License
- Bachelor of Science
Quick Apply
Program Coordinator/Clinical Supervisor
Help Group —Palmdale, CA
- $80,000 - $90,000 a year
- Full-time
- LMFT
- Licensed Clinical Social Worker
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
Clinical Systems Coordinator
Easter Seals Southern California, Inc. —Lancaster, CA
- $25 - $30 an hour
- Full-time
- Computer Science
- Clinic experience
- Mid-level
6d
Clinical Donation Coordinator I - PeeDee Region
WE ARE SHARING HOPE SC —United States
- On call
- Mid-level
- Operating room
- 2 years

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PMI Materials Coordinator (supporting the Air Force Research Lab)
ASRC Federal —Edwards AFB, CA
0-2 years of experience in materials coordination, equipment management, logistics, or related field. Create laminated index cards for relief valves, affix…
$32 an hour
Quick Apply

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Clinical Education Coordinator
Ohio University (Dublin) Physician Assistant Program —Dublin, OH
While the DCE retains responsibility for academic oversight, curricular alignment, site development strategy, and clinical decision-making, the CEC provides the…
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4d
Clinical Research Coordinator
OhioHealth —Columbus, OH
This position performs basic day to day activities related to clinical research studies including recruit and screen participants, obtains informed consent,…

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Clinical Research Sub-Investigator (NP, PA, MD, or DO)

Chemidox Clinical Trials
Lancaster, CA

Quick Apply

Job Details

Full-time
6 days ago

Benefits

Paid holidays
Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance
Opportunities for advancement
Life insurance

Qualifications

Teamwork
Electronic health records (EHR) management
Bachelor of Science
Bachelor's degree
Computer skills
Nursing
Analytics

Full Job Description

Clinical Research Sub-Investigator

Eligible Applicants: Nurse Practitioner (NP), Physician Assistant (PA), Medical Doctor (MD), or Doctor of Osteopathic Medicine (DO)

Company: Chemidox Clinical Trials

Location: Lancaster, California

Job Type: Full-Time

Schedule: Monday-Friday Onsite

Compensation: Competitive salary based on experience, qualifications, and leadership background.

About Chemidox

Chemidox Clinical Trials is seeking a motivated Nurse Practitioner (NP), Physician Assistant (PA), Medical Doctor (MD), or Doctor of Osteopathic Medicine (DO) to join our growing team as a Clinical Research Sub-Investigator.

Chemidox is a fast-growing, multispecialty clinical research organization conducting Phase II-IV clinical trials across a variety of therapeutic areas, including women's health, OB-GYN, internal medicine, cardiology, dermatology, neurology, pediatrics, vaccines, and metabolic disease. We partner with leading pharmaceutical companies and CROs to bring innovative therapies to our community while maintaining a patient-first approach.

We value visibility, ownership, teamwork, professional development, and continuous improvement. We believe strong teams are built through open communication, shared accountability, reliable follow-through, and a clear understanding of responsibilities and progress.

Position Summary

This position is designed for clinicians who want to expand beyond traditional patient care, contribute to advancing medical research, and develop as clinical leaders within a growing organization.

Working under the supervision of the Principal Investigator, you will perform protocol-required clinical assessments, protect participant safety, collaborate with research coordinators, and help ensure studies are conducted in accordance with study protocols, Good Clinical Practice (GCP), and applicable regulations.

Previous clinical research experience is preferred but not required. We provide structured onboarding, hands-on training, direct mentorship, and opportunities for long-term professional and leadership development.

Primary Responsibilities Leadership & Operations

Conduct protocol-required physical examinations and clinical assessments.
Review medical histories, medications, laboratory results, and study eligibility.
Evaluate, document, and manage adverse events and participant safety concerns.
Complete accurate clinical documentation and source records.
Maintain clear communication regarding progress, concerns, risks, and next steps.
Take ownership of assigned responsibilities and follow them through to completion.
Collaborate with Principal Investigators, study coordinators, and sponsors to ensure protocol compliance.
Participate in investigator meetings, sponsor visits, monitoring visits, and study training.
Provide clinical guidance and mentorship to research coordinators and staff.
Help develop clinical competencies across the research team.
Promote a culture of accountability, ownership, teamwork, and continuous improvement.
Follow study protocols, company SOPs, Good Clinical Practice (GCP), and all applicable regulatory requirements.
Support initiatives that improve participant safety, data quality, and operational excellence.

Qualifications

Active, unrestricted California license as an NP, PA, MD, or DO.
Graduate of an accredited Nurse Practitioner, Physician Assistant, Medical Doctor, or Doctor of Osteopathic Medicine program.
Current board certification, as applicable.
Strong clinical assessment and decision-making skills.
Excellent communication, organization, and documentation skills.
Professional, dependable, detail-oriented, and eager to learn.
Current BLS certification (or ability to obtain upon hire).
Comfortable using electronic medical records and computer-based systems.

Preferred Qualifications

Previous clinical research experience.
Good Clinical Practice (GCP) knowledge.
ACLS certification.
Bilingual in English and Spanish.
Demonstrated leadership experience managing clinical research teams.
Strong knowledge of FDA regulations, ICH-GCP, HIPAA, IRB requirements, and clinical research operations.
Proficiency with CRIO or comparable Clinical Trial Management Systems.
Strong analytical, organizational, communication, and leadership skills.
Ability to prioritize effectively in a fast-paced environment.

Nurse Practitioners, Physician Assistants, Medical Doctors, and Doctors of Osteopathic Medicine are encouraged to apply.

Who Will Thrive in This Role

We're looking for someone who:

Thrives in a fast-paced, growing organization.
Takes ownership and consistently follows through.
Communicates proactively and maintains visibility regarding progress, challenges, and solutions.
Enjoys learning and continuous improvement.
Thinks critically and helps solve problems.
Works collaboratively within a multidisciplinary team.
Demonstrates professionalism, integrity, and sound clinical judgment.
Builds trust with patients, physicians, sponsors, and colleagues.
Values accountability, teamwork, and personal growth.
Wants to grow into a clinical leadership role within an expanding research organization.

What We Offer

Structured clinical research onboarding and training.
Direct mentorship from experienced Principal Investigators.
Exposure to studies across multiple therapeutic areas.
Ongoing coaching, feedback, and professional development.
Collaborative, transparent, and team-oriented culture.
Opportunities to advance into senior clinical and leadership positions.
Health, dental, and vision insurance.
Paid time off and paid holidays.
Competitive compensation based on experience and qualifications.

Equal Opportunity Employer

Chemidox Clinical Trials is an Equal Opportunity Employer. Qualified applicants will receive consideration for employment without regard to any characteristic protected by applicable federal, state, or local law.

How to Apply

Please submit your resume along with a brief statement describing your interest in clinical research and your long-term professional goals.

Benefits:

401(k)
Dental insurance
Health insurance
Life insurance
Paid time off
Vision insurance

Work Location: In person

Quick Apply

Refine Your Search

clinical research coordinator jobs in lancaster, ca

Clinical Research Sub-Investigator (NP, PA, MD, or DO)

PMI Materials Coordinator (supporting the Air Force Research Lab)

Quality Clinical Safety Coordinator - Quality Mgmt/Clinical Safety - Full Time/Days - Req#2117934814

Hazardous Materials Coordinator (supporting the Air Force Research Lab)

Clinical Training & Skills Development Coordinator CCU - Education - Full Time/Days - Req #211796693

Program Coordinator/Clinical Supervisor

Clinical Systems Coordinator

Clinical Donation Coordinator I - PeeDee Region

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