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Entry Level Clinical Data Standards Jobs (NOW HIRING)

EDETEK

Clinical Data Analyst

Princeton, NJ · On-site

He/she will ensure that processes and protocols are followed, regulations and company standards are followed, and the analysis goals are achieved, with quality and efficiency. A Clinical Data Analyst ...

EDETEK

Clinical Data Analyst

Princeton, NJ · On-site

He/she will ensure that processes and protocols are followed, regulations and company standards are followed, and the analysis goals are achieved, with quality and efficiency. A Clinical Data Analyst ...

Tranquil Clinical Research

Research Intern

Webster, TX · On-site

Description The Research Intern is an entry level clinical research position. The Intern will ... The Research Intern will also form other duties such as data entry, and administrative duties such ...

Belay Diagnostics

Clinical Data Abstractor

Chicago, IL · On-site

$50K - $70K/yr

This position is responsible for abstracting key clinical data from electronic health records, preparing standardized case documentation, maintaining laboratory databases, ensuring required ...

Belay Diagnostics

Clinical Data Abstractor

Chicago, IL · On-site

$50K - $70K/yr

This position is responsible for abstracting key clinical data from electronic health records, preparing standardized case documentation, maintaining laboratory databases, ensuring required ...

Honorhealth

Clinical Data Abstractor II

Scottsdale, AZ · Remote

Maintains established productivity standards * Maintains competency in measure and/or registry ... to clinical data abstractor lead and/or director in a timely manner. * Established effective ...

New

Collabera

Clinical Data Manager

Irvine, CA

Clinical Data Manager Location: Irvine, CA USA 92618 Duration: 12 months (Strong Possibility of ... flowcharts, Standard Operating Procedures (SOP), work instructions, training guidelines, etc.

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Clinical Data Analyst

EDETEK

Princeton, NJ • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 10 days ago

Job description

A Clinical Data Analyst (or Clinical Informatics Analyst) is a clinical research information professional responsible for verifying the validity of clinical trials and data gathered. He/she will ensure that processes and protocols are followed, regulations and company standards are followed, and the analysis goals are achieved, with quality and efficiency.

A Clinical Data Analyst’s primary responsibility is to ensure that data is accurate and reliable throughout the clinical trial conduct, analysis, and regulatory submission. The information collected and produced is free of errors, relevant, and sound. All in all, a Clinical Data Analyst is at the center of data management for an organization, right from planning and execution to completion of a clinical study phase.

Essential Functions and Responsibilities
  • validating results and conclusions from clinical research
  • overseeing external and internal data management activities
  • expanding or modifying the system to serve new purposes and improve workflow
  • designing clinical and administrative reports
  • reviewing, extracting, compiling, and analyzing study data for compliance, quality, and accuracy, and undertaking quality improvement initiatives
  • coordinating with other relevant departments (e.g., study management team, clinical operations, clinical data management, and biostatistics) to determine the areas to be analyzed and see that appropriate measures are taken to ensure data analysis is useful
  • identifying necessary resources, developing plans for data-related projects, and determining timelines and milestones
  • performing data validation, data reconciliation, and data surveillance
  • conducting training for technical and software programs

Requirements

Education and Experience Required

  • Ability to compile, code, and categorize data
  • Ability to handle multiple priorities and explore innovative solutions to problems
  • Strong interpersonal and communication skills
  • Tackling complex situations involving study management and conduct teams, clinical data management, biostatisticians, and regulatory agencies.
  • Creative thinking, an eye for detail, working independently.

Ability to compile, code, and categorize data

  • Ability to handle multiple priorities and explore innovative solutions to problems
  • Strong interpersonal and communication skills
  • Tackling complex situations involving study management and conduct teams, clinical data management, biostatisticians, and regulatory agencies.
  • Creative thinking, an eye for detail, working independently

Benefits

Benefits vary by country, but remain competitive. Below is a sample of the benefits offered to U.S. employees.

  • Choice of comprehensive Medical, Vision and Dental Insurance plans
  • Paid vacation time and sick days
  • Corporate holidays annually
  • Participation in the 401K Plan
  • Comprehensive perks and discount programs for AAA, wholesale, insurance, Rx, fitness, pets, entertainment, etc.
  • Health Advocate and Employee Assistance Program
Location

Princeton, NJ preferred; applicants based in Brazil and Argentina are also encouraged to apply.

Equal Opportunity Employer Statement

EDETEK is an equal opportunity employer and does not unlawfully discriminate against employees or applicants for employment on the basis of an individual’s race, color, religion, creed, sex, national origin, age, disability, marital status, veteran status or any other status protected by applicable law. This policy applies to all terms, conditions and privileges of employment, including recruitment, hiring, placement, compensation, promotion, discipline, and termination. Whenever possible, the company makes reasonable accommodations for qualified individuals with disabilities to the extent required by law.

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About Edetek

Sourced by ZipRecruiter

Industry

Software development

Company size

201 - 500 Employees

Headquarters location

Princeton, NJ, US

Year founded

2009

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