Clinical Data Analyst Resume Samples - Page 2

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Clinical Data Analysts determine the efficiency of clinical trials and assess data. Common work duties listed on a Clinical Data Analyst resume are performing statistical analysis, checking data integrity, updating databases, providing feedback, implementing clinical system requirements, and testing protocols. Based on our collection of example resumes, these experts should showcase throughout their job applications computer proficiency, clinical data familiarity, statistics expertise, communication and interpersonal skills, and time management. Successful candidates hold a Bachelor's Degree in life sciences or information technology.

For more information on what it takes to be a Clinical Data Analyst, check out our complete Clinical Data Analyst Job Description.

11

Clinical Data Analyst

Transitioned existing health Access DB to McKesson Home Health Software for Clinical and Agency Management

  • Educated and trained end users on computer applications to collect and distribute patient scheduling, billing and payroll data, billing history information in McKesson Empowering Healthcare system.
  • Optimized system performance during user data and payroll transaction generation.
  • Using Crystal Reports, generated reports that allowed management to make informed decisions based on customer invoices, billing statements, and statistics.
  • Customized databases and imported tables from databases to allow users to generate queries and custom reports. Responsible for day to day operation and maintenance of software.
Candidate Info
19
years in
workforce
1
year
at this job
12

Clinical Data Analyst

Maintained coherence between CRFS and the organization's own MS SQL Server based database from study initiation to closure

  • Wrote the review guidelines and edit specifications for a Phase II Pulmonary study
  • Created test data for database and performed edit validation at the initiation of a Phase III GI study
  • Developed queries in SQL and Access to extrapolate requested data in report format from the database
  • Liaison to departments regarding data entry and edit guideline issues from pre-database development to post live
Candidate Info
9
years in
workforce
10
months
at this job
C
Computer Programming
BSN
Nursing
Health Administration
13

Clinical Data Analyst

Worked with the Chief Clinical Information Officer in the development of business specifications for product enhancement and new product/view design.

  • Collected business intelligence from all applicable sources, including but not limited to, internal customers (e.g., customer development, sales, and marketing), national publications and references, regulatory standards and healthcare accreditation guidelines).
  • Documented catalogs, cross-references and maintains business requirements and their relationships to the original sources.
  • Analyzed requirements from multiple sources and current product data and views and propose enhancements and/or solutions to update product(s) to meet the requirements.
  • Collaborated with customer development and sales staff to fully understand customer needs.
  • Managed research projects and data documentation projects from conception to completion.
  • Discovered, recognized and identified potential areas where new requirements and information is made available that might impact current products/views of the data.
  • Managed the process for the IHM Elearning Program and achievement/maintenance of ANCC provider status.
Candidate Info
7
years in
workforce
1
year
at this job
BS
Business Administration
MS
Health Care Administration
14

Sr. Clinical Data Analyst & Clinical Data Analyst

Successfully served as Data Management Project Lead within a team setting, managing all DM activities for Phase I, II, III & IV clinical trials

  • Trained DM personnel in department procedures and practices
  • Designed, built, tested & documented study databases and edit check programs
  • Developed data entry plan and trained data entry staff on its use
  • Coded Adverse Events, Concomitant Medications and Medical History
Candidate Info
15
years in
workforce
4
years
at this job
BA
Psychology
15

Clinical Data Analyst I

Reviewed protocols, designed case report forms, reviewed case report forms and documented data problems.

  • Created and maintained clinical databases by using SAS and CLINTRIAL.
  • Developed and maintained SAS programs for edit checking and produced data listings.
  • Created queries using SQL*PLUS.
  • Monitored the progress of data entry, and modified data entry screen design performed by Clinical Data Technicians.
  • Participated in CANDA validation for the Neuromuscular Blocker group.
  • Interacted with relevant clinical research personnel.
Candidate Info
1
year in
workforce
11
months
at this job
BS
Public Health
16

Clinical Data Analyst III

Utilizing SAS, provided customized statistical tables, listings and graphs for the statistical section of New Drug Applications.

  • Designed and assessed statistical analysis tables for efficacy and laboratory values.
  • Created SAS data sets from an ORACLE database.
  • Interacted with Clinical Research personnel to design and generate laboratory reports for the safety section of New Drug Applications.
  • Performed final quality reassurance checks of efficacy data.
  • Organized and chaired meetings to coordinate data collecting, handling, and analysis.
Candidate Info
5
years in
workforce
5
years
at this job
BS
Mathematics
17

Clinical Data Analyst Clinical Quality Assurance

Reviewed case report forms generated from clinical trials for completeness and accuracy using edits and current case report forms listings.

  • Performed manual and programmatic validation review of all incoming data and case report forms. This included annotate case report forms.
  • Generated data clarification forms if data is incomplete, unclear, or discrepant.
  • Updated the database through SAS reported daily maintenance updates as a result of the answered data clarification forms (DCF's) case listing of edits output.
  • Analyzed laboratory results for accuracy and completeness.
  • Reviewed data management plan daily.
Candidate Info
11
months in
workforce
3
months
at this job
AA
Associate of Arts
18

Clinical Data Analyst Clinical Quality Assurance

Reviewed case report forms generated from clinical trials for completeness and accuracy using edits and current case report forms listings.

  • Performed manual and programmatic validation review of all incoming data and case report forms. This included annotate case report forms.
  • Generated data clarification forms if data is incomplete, unclear, or discrepant.
  • Updated the database through SAS reported daily maintenance updates as a result of the answered data clarification forms (DCF's) case listing of edits output.
  • Analyzed laboratory results for accuracy and completeness.
  • Reviewed data management plan daily.
Candidate Info
11
months in
workforce
3
months
at this job
19

Clinical Data Analyst

Meticulously reviewed Case Report Forms (CRFs) in accordance with the clinical protocol, departmental specifications, and ICH/GCP guidelines.

  • Generated Data Clarification Forms (DCFs) if data was incomplete, unclear, or discrepant according to the validation specifications of the Data Management Plan (DMP).
  • Updated the database and CRFs as a result of answered DCFs.
  • Extensive experience with data cleaning, query writing, and query application using Oracle Clinical 4.0.3.
Candidate Info
1
year in
workforce
1
year
at this job
BS
Biology
MA
Public Health
20

Clinical Data Analyst

Responsible for study management and data management on multiple clinical trials.

  • Managed the workflow of clinical sites world wide to issue data queries and coordinate return of data.
  • Collected and reviewed the data of multiple, simultaneous studies and maintained data query results.
  • Interfaced between the sites and the sponsor, escalated issues when necessary. Maintained contact lists for study locations. Conducted outreach to sites when needed.
  • Collected and reviewed FDA mandated regulatory documents for clinical trial master files.
  • Reviewed and gave sponsor approval of sites' informed consents for each study prior to IRB submission.
  • Conducted meetings and other administrative tasks as needed.
Candidate Info
5
years in
workforce
1
year
at this job
BS
Computational Math And Sciences

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