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Berman Clinical Jobs in California (NOW HIRING)

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Berman Clinical information

What is a Berman Clinical job?

Berman Clinical jobs typically refer to positions at Berman Clinical, a company specializing in clinical research and trial management. Roles at Berman Clinical may include clinical research coordinators, research assistants, and support staff who help conduct and manage medical studies. Employees are involved in tasks such as patient recruitment, data collection, regulatory compliance, and coordinating with healthcare professionals. Working at Berman Clinical provides an opportunity to contribute to the advancement of medical research and patient care.

What skills and qualifications are needed to thrive as a Clinical Research Coordinator at Berman Clinical?

To thrive as a Clinical Research Coordinator at Berman Clinical, you need a background in life sciences, attention to detail, and experience with clinical trial protocols, often supported by a bachelor’s degree or higher in a relevant field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications such as ACRP or SOCRA are typically required. Strong organizational skills, communication, and the ability to multitask make someone stand out in this position. These skills ensure accurate data management, regulatory compliance, and effective collaboration, all of which are crucial for the successful execution of clinical trials.

What are common challenges faced by clinicians at Berman Clinical, and how can new hires navigate them?

Clinicians at Berman Clinical often encounter challenges such as managing a diverse patient caseload, staying updated with the latest treatment protocols, and balancing administrative duties with direct patient care. New hires can successfully navigate these challenges by actively participating in regular team meetings, seeking mentorship from experienced colleagues, and utilizing the clinic's ongoing professional development resources. Strong collaboration and open communication with interdisciplinary team members also help ensure high-quality patient outcomes and a supportive work environment.

What is the difference between Berman Clinical vs Berman Medical Assistant?

AspectBerman ClinicalBerman Medical Assistant
Required CredentialsCertification or training in clinical proceduresCertified Medical Assistant (CMA) or equivalent
Work EnvironmentClinics, hospitals, healthcare facilitiesDoctor's offices, clinics, outpatient settings
Employer & IndustryHealthcare providers, hospitals, clinicsMedical practices, outpatient clinics
Common Search/ComparisonClinical duties, patient care, certificationsMedical assisting, clinical tasks, certification requirements

Both Berman Clinical and Berman Medical Assistant roles involve patient care and clinical tasks within healthcare settings. However, Berman Clinical typically emphasizes more advanced clinical procedures and may require specific certifications, while Berman Medical Assistant focuses on assisting physicians with both administrative and clinical duties. Understanding these differences helps job seekers identify the role that best matches their skills and career goals.

What are popular job titles related to Berman Clinical jobs in California?

For Berman Clinical jobs in California, the most frequently searched job titles are:

What job categories do people searching Berman Clinical jobs in California look for?

The top searched job categories for Berman Clinical jobs in California are:

What cities in California are hiring for Berman Clinical jobs?

Cities in California with the most Berman Clinical job openings:

Berman Clinical jobs near you

Clinical Research Associate I - Heart Institute - Berman Lab

Cedars Sinai

Los Angeles, CA • On-site

$25 - $33.51/hr

Full-time

Re-posted 23 days ago

Cedars-Sinai rating

8.6

Company rating: 8.6 out of 10

Based on 131 frontline employees who took The Breakroom Quiz

43rd of 1,060 rated hospitals

Job description


Grow your career at Cedars-Sinai!
Cedars-Sinai Medical Center has been named to the Honor Roll in U.S. News & World Report's "Best Hospitals 2025-2026" rankings. When you join our team, you'll have access to groundbreaking biomedical research facilities and world-class medical education programs. We take pride in hiring exceptional, dedicated professionals who are passionate about advancing healthcare. Our physicians, nurses, and staff reflect the culturally and ethnically diverse communities we serve and are united by a shared commitment to excellence. Together, we foster a dynamic, inclusive environment that drives innovation and supports the gold standard of patient care.
Are you ready to be a part of breakthrough research?
The Smidt Heart Institute reflects Cedars-Sinai's steadfast dedication to heart disease and research innovation giving patients access to the highest level of care. Year after year, thousands of people trust their hearts to Smidt Heart Institute at Cedars-Sinai. Our cardiologists, cardiac surgeons and niche care teams treat the full spectrum of heart disease and disorders, while our investigators continue to advance the field with groundbreaking, life-saving research. From genetic counseling and targeted drug therapies to a growing array of minimally invasive procedures, Cedars-Sinai continues to stand at the forefront of technology, innovation and discovery improving patient outcomes.
What will you be doing in this role?
The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Evaluates and abstracts research data and ensures compliance with protocol and research objectives. Responsible for completing case report forms, entering clinical research data, and assist with regulatory submissions to the IRB. Provides limited patient contact as needed for study and assist with study budget and patient research billing. Ensures compliance with all federal, local, FDA, IRB, and HIPAA guidelines and regulations pertaining to the study and patient care.
Primary Duties & Responsibilities:
  • Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement study.
  • Evaluates and abstracts clinical research data from source documents.
  • Ensures compliance with protocol and overall clinical research objectives.
  • Completes Case Report Forms (CRFs).
  • Enters clinical research data into Electronic Data Systems (EDCs) that the sponsors provide.
  • Provides supervised patient contact or patient contact for long term follow-up patients only.
  • Assists with regulatory submissions to the Institutional Review Board (IRB) including submission of Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines.
  • Assists with clinical trial budgets.
  • Assists with patient research billing.
  • Schedules patients for research visits and research procedures.
  • Responsible for sample preparation and shipping and maintenance of study supplies and kits.
  • Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.
  • Maintains research practices using Good Clinical Practice (GCP) guidelines.
  • Maintains strict patient confidentiality according to HIPAA regulations and applicable law.
  • Participates in required training and education programs.

Qualifications
Education:
  • High School Diploma is required. Bachelor's degree is preferred in Science, Sociology, or a related field.

Experience and Skills:
  • One (1) year of clinical research related experience is preferred.

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