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Clinical Research Data Associate II - The Angeles Clinic & Research Institute

Cedars-Sinai886 open roles

Where
Los Angeles, CA, United States
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Your applicationOpen nowClinical Research Data Associate II - The Angeles Clinic & Research InstituteCedars-Sinai · Los Angeles, CA, United States

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The clock on this job

Early applications get read.

13.3% of postings close within 7 days. Measured by our own scanner across the market. Cedars-Sinai postings stay open a median of 14 days.

Share of postings closed within
  1. 2.1%1 day
  2. 4.6%3 days
  3. 13.3%7 days
  4. 21.3%14 days
  5. 35.7%30 days
  6. 59.1%60 days
This job: posted yesterday

Cedars-Sinai median: 14 days open

The posting

Job Description

Why Cedars-Sinai?

At Cedars-Sinai, we pride ourselves on our inclusive and collaborative culture. We are committed to encouraging an environment where diverse perspectives are valued and innovative ideas can flourish. Our team works together to achieve world-class results, and we support each other in reaching our full potential. If you are looking to grow your career in a place that values excellence and impact, Cedars-Sinai is the perfect place for you.

Join us in our mission to transform healthcare and improve patient outcomes. Apply today and become part of a team that is making a real difference in the world!

Grow your career at Cedars-Sinai!

The Angeles Clinic & Research Institute has established an international reputation for developing new cancer therapies, providing the best in experimental and traditional treatments, and expertly guiding and training the next generation of clinicians. Our board-certified fellowship-trained medical oncologists, surgeons, immunotherapists, pathologists, and dermatologists work closely together to advance cancer care. We are committed to bringing innovative therapeutic options to all of our patients with cancer.

Join our team and contribute to groundbreaking research!

The Clinical Research Data Associate II manages the data for assigned research studies. This will include, designing forms for data collection, clinical data abstraction, processing data, maintaining record systems, and producing project reports for studies. In addition, may train clinical research staff, perform basic statistical analysis, and work with bioinformatics to develop and maintain trial management systems. Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.

Key Responsibilities:

  • Coordinates data for research studies.
  • Designs forms for data collection.
  • Performs clinical data collection/abstraction.
  • Processes clinical data using a range of computer applications and database systems to support cleaning and management of subject or patient data.
  • Produces project reports.
  • Performs data searches and other related administrative tasks.
  • Participates in required training and education programs.
  • Works closely with study monitors to review study data and respond to inquiries.
  • Provides support and preparation for study audits.
  • May train clinical research staff to help improve the quality of the data being collected.
  • May solve operational/data problems in consultation with other employees and/or supervisors.
  • May perform basic statistical analysis in conjunction with a biostatistician.

Work Location: This is a hybrid position requiring 4 days per week onsite and 1 day per week remote. Please note that fully remote work arrangements are not available for this position at this time.

Qualifications

Education

  • High School Diploma or GED required
  • Bachelor’s degree in a related field (e.g., Life Sciences, Health Sciences, or similar) preferred

Experience

  • Minimum of two (2) years of relevant experience in clinical research or a related setting
  • Hands-on experience with Electronic Data Capture (EDC) systems, preferably within oncology clinical trials
  • Familiarity with EDC platforms such as REDCap, Oracle Clinical, Veeva Vault, Medidata Rave, and/or OpenClinica
  • Proficiency with data management software and related tools
  • Demonstrated ability to work effectively in a collaborative, team-oriented environment
  • Strong attention to detail with excellent organizational and time-management skills
  • Excellent written and verbal communication skills
  • Proven ability to adhere to regulatory requirements and ethical guidelines

Licensure/Certification

  • Certification in Clinical Research (ACRP, SOCRA, or equivalent) preferred
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