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Clinical Research Relocation Jobs in California (NOW HIRING)

Clinical Research Manager

Huntington Beach, CA ยท On-site

$110K - $150K/yr

As a Clinical Research Manager, you will own end-to-end US IDE study operations, leading a team of ... Relocation benefits are not available for this posting. Apply today and be part of something ...

Clinical Research Manager

Huntington Beach, CA ยท On-site

$110K - $150K/yr

As a Clinical Research Manager, you will own end-to-end US IDE study operations, leading a team of ... Relocation benefits are not available for this posting. Apply today and be part of something ...

CLINICAL RESEARCH COORDINATOR II

Long Beach, CA ยท Hybrid

$25.50 - $34/hr

Summary The Clinical Research Coordinator II (CRC II) is a second level in the CRC career path ... Relocation assistance may be provided. These positions work closely with patients, patient families ...

CLINICAL RESEARCH COORDINATOR II

Long Beach, CA ยท Hybrid

$25.50 - $34/hr

Summary The Clinical Research Coordinator II (CRC II) is a second level in the CRC career path ... Relocation assistance may be provided. These positions work closely with patients, patient families ...

CLINICAL RESEARCH COORDINATOR I

Long Beach, CA ยท Hybrid

$25.50 - $34/hr

As a Moffitt Clinical Research Coordinator, you'll bring hope to patients by delivering tomorrow ... Relocation assistance may be provided. These positions work closely with patients, patient families ...

CLINICAL RESEARCH COORDINATOR I

Long Beach, CA ยท Hybrid

$25.50 - $34/hr

As a Moffitt Clinical Research Coordinator, you'll bring hope to patients by delivering tomorrow ... Relocation assistance may be provided. These positions work closely with patients, patient families ...

CLINICAL RESEARCH COORDINATOR I

Long Beach, CA ยท Hybrid

$25.50 - $34/hr

As a Moffitt Clinical Research Coordinator, you'll bring hope to patients by delivering tomorrow ... Relocation assistance may be provided. These positions work closely with patients, patient families ...

CLINICAL RESEARCH COORDINATOR I

Long Beach, CA ยท Hybrid

$25.50 - $34/hr

As a Moffitt Clinical Research Coordinator, you'll bring hope to patients by delivering tomorrow ... Relocation assistance may be provided. These positions work closely with patients, patient families ...

CLINICAL RESEARCH COORDINATOR I

Long Beach, CA ยท Hybrid

$25.50 - $34/hr

As a Moffitt Clinical Research Coordinator, you'll bring hope to patients by delivering tomorrow ... Relocation assistance may be provided. These positions work closely with patients, patient families ...

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Showing results 1-20

Clinical Research Relocation information

What are some common challenges clinical research professionals face when relocating for a new position, and how can they prepare?

Relocating for a clinical research role often involves adjusting to new regulatory environments, learning institutional protocols, and building relationships with unfamiliar site teams. It can be challenging to quickly integrate into established workflows and local cultures, especially when overseeing multiple research sites or adapting to varying patient populations. To prepare, candidates should research the local regulatory landscape, reach out to future colleagues ahead of time, and seek support from their employer's HR or relocation services to ensure a smoother transition.

What is the difference between Clinical Research Relocation vs Clinical Research Coordinator?

AspectClinical Research RelocationClinical Research Coordinator
CredentialsTypically requires experience in clinical research, sometimes certifications like CCRPRequires knowledge of clinical trial protocols, often a degree in health sciences or related field
Work EnvironmentInvolves managing logistics of relocating research staff or sites, often travel and coordinationWorks directly with patients, investigators, and study teams at research sites
Employer & Industry UsageUsed by research organizations, pharmaceutical companies, and CROs for site or staff movementCommonly employed at hospitals, research centers, and clinical trial sites

Clinical Research Relocation focuses on managing the logistics of moving research staff or sites, while Clinical Research Coordinators handle day-to-day trial operations at research sites. Both roles require knowledge of clinical research processes but serve different functions within the industry.

What is clinical research relocation?

Clinical research relocation refers to the process of moving clinical research operations, staff, or study participants from one location to another. This may occur due to regulatory requirements, expansion, or to access better facilities and patient populations. Relocation requires careful planning to ensure compliance with protocols, maintain data integrity, and minimize disruption to ongoing studies. It also often involves logistical coordination, regulatory approvals, and communication with stakeholders. In some cases, relocation support is provided to research staff or participants to facilitate the transition.

What are the key skills and qualifications needed to thrive in clinical research relocation, and why are they important?

To thrive in Clinical Research Relocation, you need a background in clinical research, project management, and regulatory compliance, often supported by a relevant life sciences degree. Familiarity with clinical trial management systems (CTMS), standard operating procedures (SOPs), and knowledge of Good Clinical Practice (GCP) guidelines is essential. Strong organizational skills, adaptability, and effective communication are critical for coordinating logistics and ensuring smooth transitions for studies, staff, or participants. These skills ensure regulatory adherence, minimize disruptions, and support the seamless execution of clinical research activities during relocation processes.
What cities in California are hiring for Clinical Research Relocation jobs? Cities in California with the most Clinical Research Relocation job openings:
Infographic showing various Clinical Research Relocation job openings in California as of August 2026, with employment types broken down into 94% Full Time, and 6% Contract. Highlights an 88% In-person, and 12% Hybrid job distribution.

Clinical Research Manager

BiVACOR Inc

Huntington Beach, CA โ€ข On-site

$110K - $150K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 12 days ago


Job description

Help Us Build the Future of the Human Heart.
At BiVACOR, we're developing the world's most advanced total artificial heart, a technology capable of saving millions of lives around the world. We're a team united by purpose, working on something truly unprecedented. Every site you activate, every team member you develop, and every data point you interpret plays a direct role in giving patients another shot at life. If that's the kind of work that gets you out of bed in the morning, we think you belong here.
About the Role
This is a senior, high-impact leadership role at the center of BiVACOR's US clinical program, where your expertise will shape how we conduct, manage, and report on one of the most groundbreaking medical device studies of our time. As a Clinical Research Manager, you will own end-to-end US IDE study operations, leading a team of clinical research professionals, ensuring regulatory compliance across all active sites, and driving the clinical strategy that will help bring the world's first Total Artificial Heart to patients who need it most. You will bring deep clinical trial expertise, strong leadership instincts, and the scientific acumen to translate complex data into compelling, accurate clinical narratives.
Key Responsibilities
  • Manage all US IDE clinical study operations including site activation, enrolment, and monitoring
  • Lead and develop a team of Clinical Research Specialists/Site Managers and Clinical Research Associates
  • Ensure US sites maintain GCP compliance, FDA regulations, and protocol adherence
  • Serve as the primary liaison with US IRBs, site Principal Investigators, and study coordinators
  • Maintain the Trial Master File per ICH E6(R2) and ISO 14155:2020; prepare for and support inspections and audits
  • Collaborate on clinical strategy and author key clinical documents including clinical study protocols, clinical study reports, clinical evaluation plans/reports, annual progress reports, risk-benefit analyses, and clinical marketing materials
  • Develop a deep understanding of clinical data; interpret and communicate complex results in a clear, concise, and scientifically accurate manner across a wide range of audiences

What You Bring
  • Bachelor's degree in Life Sciences, Nursing, Biomedical Engineering, or a related field; advanced degree preferred
  • 5+ years of clinical research experience in a medical device or pharmaceutical environment, with at least 3 years in a management or team leadership role
  • Extensive experience managing US IDE studies; thorough knowledge of FDA regulations (21 CFR 812), ICH E6(R2) GCP, and ISO 14155:2020
  • Demonstrated experience authoring regulatory and clinical documents including protocols, CSRs, CEPs/CERs, and annual progress reports
  • Strong data interpretation skills with the ability to synthesize complex clinical results and present them clearly to scientific, regulatory, and lay audiences
  • Prior experience with cardiac or implantable device studies strongly preferred; Class III medical device experience an advantage
  • Can-do attitude, strategic thinker with strong leadership and cross-functional communication skills
  • Willingness to travel to US clinical sites and attend key meetings and conferences as required

What We Offer
BiVACOR offers a competitive compensation package and comprehensive benefits, including:
  • 401(k) with company matching
  • Medical, dental, and vision insurance
  • Health Savings Account (HSA) & Flexible Spending Account (FSA)
  • Life insurance & Employee Assistance Program
  • Generous paid time off

This role may be based at BiVACOR's Huntington Beach headquarters. The expected salary range for this position based in Huntington Beach California is $110,000 - $150,000. Actual compensation will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below. Relocation benefits are not available for this posting.
Apply today and be part of something extraordinary.
BiVACOR is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.