Clinical Research Data Specialist III - Heart Institute - Bairey-Merz Lab
Cedars-Sinai · Los Angeles, California
What the posting says
Each fact carries its state:Statedfound in the postingConflictstwo statements disagree, both quotedNot mentionedthe posting does not say
- Employment typeStated
- Full time
- ExperienceStated
- 5-10 years
- EducationStated
- ['bachelor degree', 'professional certificate']
Not mentioned in this posting
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- PayNot mentioned
- The posting does not say
- Work arrangementNot mentioned
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- ShiftNot mentioned
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- Visa sponsorshipNot mentioned
- The posting does not say
Requirements, each with its sentence from the posting
These are the employer’s words. The index does not judge whether you meet them.
- Bachelor's degree in related fieldrequired
Bachelor's Degree BA/BS degree in related field of research.- required
from the posting - Experience in related field of researchrequired
4 years Experience in related field of research. - required
from the posting - Clinical data abstractionrequired
clinical data abstraction, processing data, maintaining record systems
from the posting - Data management and analysisrequired
Independently manages and maintains research data to ensure accuracy, integrity, and security
from the posting - FDA and IRB compliancerequired
Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.
from the posting - HIPAA regulationsrequired
Maintains strict patient confidentiality according to HIPAA regulations and applicable law.
from the posting - Good Clinical Practice (GCP) guidelinesrequired
Maintains research practices using Good Clinical Practice (GCP) guidelines.
from the posting - Statistical analysisrequired
may perform complex statistical analysis for publication
from the posting - Supervision and trainingrequired
Supervises clinical research staff or clinical data managers.
from the posting - Clinical Research Certification (ACRP/SoCRA)preferred
Certification In Clinical Research - preferred ACRP/SoCRA (or equivalent) certification preferred.
from the posting
Read the full posting as the employer wrote it
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.
Are you ready to be a part of breakthrough research?
The Clinical Research Data Specialist III manages the data for assigned research studies at a senior level. 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 supervise clinical research staff or clinical data managers, perform complex statistical analysis, and work with bioinformatics to develop and maintain trial management and validation systems. Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board.
- Supervises clinical research staff or clinical data managers.
- Solves operational/data problems in consultation with other employees and/or supervisors.
- In conjunction with a biostatistician, may perform complex statistical analysis for publication.
- Works with bioinformatics in the development and maintenance of clinical trials management systems including validation of systems.
- Trains clinical research staff on data collection standards, protocol requirements, and data entry systems to promote accuracy and consistency in research data.
- Independently manages and maintains research data to ensure accuracy, integrity, and security of complex, large, computerized records systems. This includes performing data searches and other related administrative tasks.
- Prepares project reports and performs statistical analysis in conjunction with a biostatistician, interpreting and presenting findings to support study objectives and data quality initiatives.
- Processes clinical data using a range of computer applications and database systems to support cleaning and management of subject or patient data.
- Performs clinical data collection, abstraction, targeted data searches to support accurate and timely data availability for study objectives.
- Understands regulations, policies, protocols and procedures to control and maintain accurate records .
- 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
- Bachelor's Degree BA/BS degree in related field of research.- required
Experience
- 4 years Experience in related field of research. - required
Licenses and Certifications
- Certification In Clinical Research - preferred ACRP/SoCRA (or equivalent) certification preferred.
The posting text is reproduced as the employer wrote it; the index adds nothing to it.