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Crc Assistant Jobs (NOW HIRING)

CenExel

Clinical Rater

Seal Beach, CA · On-site

$85K - $120K/yr

Complete Study Guides and Study Launch with CRC * Assist team in management and assessment of adverse events * Ensure safety of subjects * Assist with recruitment efforts * Mentor staff, as needed

CRC Group

Escrow Assistant

Fort Worth, TX · On-site

$18.75 - $23.75/hr

... experienced Escrow Assistants with a positive attitude to be a part of our team. This is an ... At CRC Group, we're committed to supporting every aspect of teammates' well-being - physical ...

CenExel

Clinical Rater

Los Alamitos, CA · On-site

$85K - $120K/yr

Complete Study Guides and Study Launch with CRC * Assist team in management and assessment of adverse events * Ensure safety of subjects * Assist with recruitment efforts * Mentor staff, as needed

CRC Group

Broker Assistant

Dallas, TX · On-site

... The Broker Assistant supports brokerage outcomes by coordinating market-facing activity and ... At CRC Group, we're committed to supporting every aspect of teammates' well-being - physical ...

CRC Group

HR Coordinator

New York, NY · On-site

$65K - $80K/yr

Core Responsibilities HR Operations & Employee Support • Assist as a resource for employee ... At CRC Group, we're committed to supporting every aspect of teammates' well-being - physical ...

CRC Group

HR Coordinator

Manhattan, NY

$65K - $80K/yr

Core Responsibilities HR Operations & Employee Support • Assist as a resource for employee ... At CRC Group, we're committed to supporting every aspect of teammates' well-being - physical ...

CRC Group

Associate Broker

Redondo Beach, CA · On-site

$80K - $95K/yr

... 7. Assist broker with meeting or exceeding production goals as assigned by CRC. 8. Maintain current knowledge of the insurance industry and sales ideas through regular attendance at workshops ...

CRC Group

Account Executive

Birmingham, AL · On-site

... Assist and/or provide quotations for new business, renewals and endorsements through managing all ... At CRC Group, we're committed to supporting every aspect of teammates' well-being - physical ...

CRC Group

Associate Broker

Seattle, WA · On-site

... 7. Assist broker with meeting or exceeding production goals as assigned by CRC. 8. Maintain current knowledge of the insurance industry and sales ideas through regular attendance at workshops ...

CRC Group

Associate Underwriter

Chicago, IL · On-site

... CRC Client). 9. Proof policies, endorsements, audits, cancellations, etc and make corrections as appropriate. Provide necessary instruction to Underwriting Assistants and Technical Assistants. 10. ...

CRC Group

Associate Broker

Redondo Beach, CA · On-site

$60K - $80K/yr

... 7. Assist broker with meeting or exceeding production goals as assigned by CRC. 8. Maintain current knowledge of the insurance industry and sales ideas through regular attendance at workshops ...

CRC Group

Associate Broker

Franklin, TN · On-site

... 7. Assist broker with meeting or exceeding production goals as assigned by CRC. 8. Maintain current knowledge of the insurance industry and sales ideas through regular attendance at workshops ...

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Crc Assistant information

What are the key skills and qualifications needed to thrive as a CRC Assistant, and why are they important?

To thrive as a CRC Assistant (Clinical Research Coordinator Assistant), you generally need a background in life sciences or healthcare, attention to detail, and familiarity with research protocols. Experience with data management systems, electronic case report forms (eCRFs), and possibly GCP (Good Clinical Practice) certification is beneficial. Strong organizational skills, effective communication, and the ability to work collaboratively are vital soft skills for this role. These competencies ensure accurate data collection, regulatory compliance, and efficient support for clinical research teams.

How does a CRC Assistant typically collaborate with research coordinators and other team members during clinical trials?

As a CRC Assistant, you will work closely with Clinical Research Coordinators, nurses, and sometimes principal investigators to ensure smooth trial operations. Your responsibilities may include scheduling patient visits, preparing documentation, managing data entry, and ensuring compliance with study protocols. Frequent communication and teamwork are essential, as you may need to relay updates, clarify procedures, or help resolve logistical challenges. This collaborative environment provides excellent learning opportunities and exposure to various aspects of clinical research.

What are CRC Assistants?

CRC Assistants, or Clinical Research Coordinator Assistants, support clinical research teams by helping with administrative tasks, data collection, participant recruitment, and maintaining study records. They work under the supervision of Clinical Research Coordinators and play a vital role in ensuring that research studies are conducted according to regulatory guidelines and protocols. Their responsibilities may also include scheduling participant visits, preparing study documentation, and communicating with participants and medical staff.

What is the difference between Crc Assistant vs Crc Coordinator?

AspectCrc AssistantCrc Coordinator
Required CredentialsHigh school diploma, certification in CRC or related fieldsHigh school diploma, CRC certification, experience in coordination roles
Work EnvironmentOffice settings, healthcare facilities, community organizationsOffice-based, healthcare settings, community outreach programs
Employer & Industry UsageHealthcare providers, insurance companies, community health programsHealthcare organizations, social services, program management
Common Search & ComparisonOften compared for entry-level roles and support functionsCompared for supervisory or program management roles

The main difference between a Crc Assistant and a Crc Coordinator lies in their responsibilities and experience level. Crc Assistants typically support daily operations and perform administrative tasks, while Crc Coordinators oversee program implementation and manage teams. Both roles require CRC certification, but Coordinators usually have more experience and a broader scope of duties.

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Crc Assistant jobs near you
Infographic showing various Crc Assistant job openings in the United States as of May 2026, with employment types broken down into 98% Full Time, and 2% Contract. Highlights an 100% Physical job distribution.
Clinical Rater

Clinical Rater

CenExel

Seal Beach, CA • On-site

$85K - $120K/yr

Other

Medical, Dental, Vision, Life, Retirement

Posted yesterday

Job description

About Us:
Each of CenExel's research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected and long-standing research facilities in the country. Specialty areas of research across our sites include Psychiatry, Acute Post Op Pain, Asian Bridging, Dermatology, GI, and Neurology. Each of our Centers of Excellence has tremendous experience and expertise in complex early phase trials, and all our sites have in-patient capability. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.
Along with an exceptional work environment that promotes teamwork, positive leadership, and optimal work-life balance, CenExel Clinical Research also provides highly competitive compensation and a generous benefits package to full time employees after 30 days of employment including Health Insurance, Dental, Vision, LTD, STD, Life Ins, and 401k.
Job Summary:
Responsible for performing various clinical and neurocognitive test evaluations and interview/ratings on study participants specific to the study protocol. To administer and score tests evaluating cognitive, neuropsychological, behavioral, and emotional status.
Compensation: $85,000 - $120,000/year, depending on experience and education.
Location: Los Alamitos, Torrance, and Garden Grove.
Essential Responsibilities and Duties:
  • Perform interview/ratings on study subjects to determine current levels of functioning and to create a clinical impression of the subject's current psychiatric state throughout the duration of the study
  • Administer neurocognitive battery in subject with different CNS indications
  • Complete subject's clinical intake forms (i.e. psychiatric history) and submit to the study team as specified
  • Assess and complete subject eligibility/screening forms and interact with medical monitor regarding subjects inquiries
  • Conduct telephone screens and pre-screen with potential study candidates
  • Become familiar with and adhere to policies and principles of confidentiality, informed consent and study subject rights
  • Become familiar with and adhere to the principles of Good Clinical Practices and general ethical guidelines, as related to clinical trials
  • Become familiar with the FDA Regulations pertaining to clinical trials
  • Review medical history with CRC information obtained at screening
  • Review and reconcile medical records received for subjects and prepare PI notes to explain discrepancies, if needed
  • Complete Study Guides and Study Launch with CRC
  • Assist team in management and assessment of adverse events
  • Ensure safety of subjects
  • Assist with recruitment efforts
  • Mentor staff, as needed
  • Assumes other duties and responsibilities as assigned. The above responsibilities are a general description of the level and nature of the work assigned to this classification and are not to be considered as all inclusive.
Education/Experience/Skills:
  • Must be able to effectively communicate verbally and in writing.
  • Master's Degree and/or Ph.D/Psy.D in Psychology, or related field required.
  • 1-2 years clinical experience with the mental health population.
  • Skill in organization and problem solving.
  • Skill in maintaining records.
  • Skill in developing and maintaining effective working relationships with study participants, families, staff and the public.
  • Ability to complete paperwork with precision and attention to detail.
  • Ability to interpret, adapt and apply guidelines and procedures.
  • Ability to work independently as well as functioning as part of a team.
  • Ability to communicate clearly both written and orally.

Working Conditions
  1. Indoor, Clinic environment.
  2. Essential physical requirements include sitting, typing, standing, walking.
  3. Lightly active position, occasional lifting of up to 20 pounds.
  4. Reporting to work, as scheduled, is essential.

CenExel Clinical Research is an Equal Opportunity Employer. All applicants will be considered for employment without regards to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or status.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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