Clinical Data Analyst Resume Samples - Page 5

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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.

41

Clinical Data Analyst Contractor

Reviewed and cleaned eCRF data on large multiple sclerosis study

  • Generated, reviewed and integrated queries
  • Generated listings utilizing Integrated Review
  • Reconciled external lab data and CRF data
  • Provided recommendations, test and perform QC on newly developed edit checks
  • Performed Database User Acceptance Testing
Candidate Info
8
years in
workforce
3
years
at this job
C
Certificate
MS
Regulatory And Clinical Research Management
42

Clinical Data Analyst (astrazeneca)

Reviewed and implemented SOPs (Standard Operating Procedures)

  • Reviewed CRFs for inconsistencies and identified items that require clarification
  • Served as back up to Senior Clinical Data Analyst for project specific tasks
  • Assisted in creating clinically appropriate edit specifications
  • Annotated CRFs with database specifications in accordance with global and local standards
Candidate Info
4
years in
workforce
4
months
at this job
MA
Master of Arts
Liberal Arts
Multimedia & Visual Communications
43

Clinical Data Analyst

Data Implementation Team member for phase III and IV trials for Cox II Inhibitor and Singulair Studies.

  • Ensured accurate case report form data entered into the Merck propriety system, paying special attention to adverse events and lab data.
  • Correlated lab values to clinical adverse events in the database to streamline reporting.
  • Performed checks to identify protocol violations for Inclusion/Exclusion criteria.
  • Reviewed entered data for quality control.
  • Made appropriate changes from queries into the database.
  • Generated queries from various checks programmed into the database.
  • Performed remote data capture user acceptance testing for newly designed data handling software. Reported updates at various project team meetings.
  • Worked with Laboratory Coordinators, Programmers, Physicians, in house CRA's, and various other members of the clinical team to maintain data integrity on an ongoing basis.
Candidate Info
2
years in
workforce
2
years
at this job
BA
Biology
44

Clinical Data Analyst I

Generated and closed queries or apply self evident corrections to the data according to the relevant guidelines.

  • Reviewed data listings on a monthly basis to find error and issue queries to ensure data accuracy.
  • Performed early and final database QC activities.
  • Attended training to comply with the SOP of each project.
  • Assisted with locking or unlocking the subjects whichever has inconsistent data, to be questioned to the sites and to be discussed with CRA's.
  • Participated in the Project Team meetings to address issues, provide status of the data cleaning/review and capture project priorities.
  • Froze and locked data as appropriate in time for statistical review, blinded interim quality review, interim and final database lock.
Candidate Info
3
years in
workforce
8
months
at this job
BS
Biotechnology
MA
Master of Arts
45

Sr. Clinical Data Analyst/biostatistical Sciences

Coordinated and reviewed clinical data for a privately owned and operated Contract Research Organization. Implementation: an independently developed online image (Visual Basic/Access) DBMS. Therapeutic areas: Infectious Disease (urinary, respiratory, and skin & skin structure), Neutropenia, Aphthous Stomatitis and Constipation/Quality of Life Survey.

  • Presented DBMS demos to prospective clients to differentiate company capabilities
  • Served as trainer for other employees
  • Established data processing procedures for the handling of CRFs; designed CRF mock-ups
  • Developed Data Review Guidelines; defined entry/review data checks; reviewed protocol drafts
  • Reviewed CRFs on-line, auto encoded & manually mapped recorded verbatims to preferred terms (WHOART/WHODRUG); executed site contact phone calls for resolution of CRF data clarifications; developed Access queries list for "back-end" data base clean-up
  • Maintained Patient Evaluability Log and payment allocation to Investigators
  • Executed source documentation and collection of CRFs at investigational site
  • Worked with Programming and Biostatistics to execute Analysis Plan specifications and to lock databases
  • Addressed ad-hoc requests from Sponsors of microbiological and clinical outcomes and forwarded identification of "patient evaluability" status and protocol exceptions
Candidate Info
4
years in
workforce
4
years
at this job
BS
Biology
46

Senior Clinical Data Analyst

Served as the team leader on the [company name] project teams and responsible for key project deliverables by developing and performing data checks on the clinical data in accordance with the study specific guidelines to ensure validity, performed quality control activities and ensured all necessary project documentation was created and filed correctly.

  • Ensured that timelines and contracts were adhered to and quality standards were met
  • Coordinated daily activities for Clinical Data Analyst
  • Performed and initiated workflow, sequence of events and processing for data testing
Candidate Info
13
years in
workforce
1
year
at this job
BA
Chemistry
BS
Biochemistry
MA
Global Management
47

Clinical Data Analyst I

Responsible for reviewing Case Report Forms from clinical sites for completeness and accuracy by using edits listings, manual review, and other appropriate guidelines.

  • Composed and generated Data Clarification Forms if data was unclear, incomplete, or with the Data Management Plan.
  • Accountable for updating the computer database with data from the Case Report Forms, answered Data Clarification Forms, patient profiles, and other reports.
  • Assisted with database lock activities.
Candidate Info
10
years in
workforce
8
months
at this job
HS
High School Diploma
AS
Liberal Arts
48

Clinical Data Analyst

Reviewed case report forms for completeness and consistency

  • Generated queries for missing and/or inconsistent data
  • Reviewed clinical protocols
  • Designed standard case report forms
  • Created SAS database and data entry screen using FSP Software
  • Created SAS error check program, AE and CONMED auto coding program, Summary Tables and Listing programs
  • Customized reporting of data using SAS proc print, proc report, and data null listings
  • Maintained in-house dictionary for specific study
Candidate Info
17
years in
workforce
7
years
at this job
MS
Plant Breeding
49

Clinical Data Analyst

As a clinical analyst, I provide operational and clinical business intelligence to regional directors and front line leaders.

  • Produce daily/weekly/monthly reports for the Health Services Organization to ensure smooth operations including patient census reports, nurse productivity stats, and clinical metrics
  • Create ad hoc reports and analyses for a wide range of internal and external customers utilizing several systems/software including SQL Server, Oracle, Excel and Access
  • Documented business and technical specifications for reporting.
  • Translated business initiatives into comprehensive reports for management.
Candidate Info
22
years in
workforce
6
years
at this job
BA
Business Administration
50

Clinical Data Analyst

Served as point person for day-to-day project activities as back-up to Lead Data Manager

  • Performed data review and query generation
  • Tracked study progress, distributed reports and generated/compiled data management statistics as relevant to the project
  • Assisted in coordinating the work of Associate Data Analysts assigned to the project
  • Defined and tested edit checks
  • Developed data entry guidelines
  • Assisted in CRF development and design
  • Interacted closely with Clinical Research Associates (CRA) in dealing with project needs as necessary
Candidate Info
6
years in
workforce
1
year
at this job
AS
Arts
AS
Science
BA
Chemistry

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