Eric Hickman

Eric Hickman Email and Phone Number

Clinical Data Manager | Data Review, Query Resolution, Reconciliation
Eric Hickman's Location
Raleigh, North Carolina, United States, United States
Eric Hickman's Contact Details
About Eric Hickman

At the forefront of Clinical Data Management for Fortrea, my focus is on ensuring the accuracy and integrity of clinical trial data, particularly in oncology studies. My tenure has honed my skills in data review, query resolution, and the successful completion of UAT for EDC systems.Leading operations teams, I adeptly oversee tasks such as SAE reconciliation and data migration while running metrics for productivity and quality. Contributing to the team's objectives, we ensure on-time delivery of precise clinical data that supports the innovation of pharmaceutical research and client satisfaction.Therapeutic Areas: Cardiovascular, Central Nervous System, Endocrinology/Metabolic, Gastrointestinal, Infectious Diseases, Men’s Health, Oncology (Solid Tumors-Lung, Breast), Orthopedics, Pediatrics, Renal, Respiratory/Pulmonary, Rheumatology/Arthritis, Urology and Women’s Health.Data Management Skills:Discrepancy Management, Data Listings Review, SAE Reconciliation, Lab Reconciliation, Vendor Reconciliation, Study Metrics, Edit Checks Review/Testing (UAT), Creation of Manual Data Listings and Generation of SAS Listings.Technical Skills:OCRDC, Rave, Inform, Veeva Vault (EDC and eTMF), SharePoint and Microsoft Office.

Eric Hickman's Current Company Details

Clinical Data Manager | Data Review, Query Resolution, Reconciliation
Eric Hickman Work Experience Details
  • Fortrea
    Associate Clinical Data Manager, Fspx
    Fortrea Oct 2021 - Nov 2023
    Durham, North Carolina, Us
    Provides regular updates to Sponsor Clinical Data Management Lead, attends Data Working Group meetings, oversee CDM offshore support by delegating and training for tasks/activities. Performs high level review of study status as assigned by the Sponsor Clinical Data Management Lead. Responsibilities include operations teams’ statuses (i.e., Coding, External Data Specialists, Data Reviewers), SAE recon, eTMF, & Data Migration. Run metrics and KPIs as appropriate for the operations team to review for productivity, quality and on time delivery.
    View
  • Labcorp Drug Development
    Clinical Data Coordinator Iii, Fspx
    Labcorp Drug Development Jan 2020 - Oct 2021
    Burlington, North Carolina, Us
    Serve as a member of the project team with primary responsibility for clinical data review, query generation / resolution and reconciliation activities to support the delivery of clinical data according to client quality and integrity specifications, and project timelines and productivity.
    View
  • Tesaro, Inc.
    Clincal Data Manager
    Tesaro, Inc. Jul 2019 - Dec 2019
    Waltham, Massachusetts, Us
    Responsibilities include Data Review for Oncology studies, Create and review data point listings to determine trends and assess data quality risks. Performs UAT on new and updated EDC systems and edit check testing. Create and maintain process specific guidelines. Perform Manual listing review for SAE and lab reconciliation. Update and maintain Protocol Deviation table, and training of new staff
    View
  • Syneos Health Clinical Solutions
    Clinical Data Associate Iii
    Syneos Health Clinical Solutions Jan 2018 - Jul 2019
    Morrisville, North Carolina, Us
    Lead Clinical Data Associate on multiple studies, which included back up to the Lead Data Manager, participated in weekly/monthly sponsor(s) meetings, delegated tasks among other CDAs assigned to studies and held weekly status/progress internal team meeting regarding certain tasks, also trained and mentored other CDAs with study tasks. Administered study database access interface based on request form workflows (EDC, SharePoint, other data systems). Performed data review to increase independence and efficiency, while complying with standard operating procedures/work instructions as well as study specific plans and guidelines. Performed essential tasks which included edit checks testing, discrepancy management, data listings review, study metrics, SAE reconciliation, vendor reconciliation, user access requests, monthly reports and additional data management tasks as requested.
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  • Inc Research
    Clinical Data Associate Iii
    Inc Research May 2016 - Jan 2018
    Raleigh, North Carolina, Us
    Performs data review with increased independence and efficiency as compared to less experienced data management roles in compliance with Standard Operating Procedures/ Work Instructions (SOPs/WIs), regulatory directives, and study specific plans and guidelines. Performs essential functions which support database testing, as well as additional data management activities such as CRF/eCRF design, external data reconciliations, and reviews of database designs within an appropriate mentoring and training program. Also provides training and work direction to data management staff as needed.
    View
  • Covance
    Clinical Data Coordinator
    Covance Nov 2015 - May 2016
    Princeton, New Jersey, Us
    Remote position whose duties include: data listings review, query creation, query resolution, & reconciliations within the Inform & Rave data platforms.
    View
  • Ppd
    Clinical Data Associate
    Ppd Sep 2015 - Sep 2015
    Wilmington, Nc, Us
    Identifies, resolves, and updates data discrepancies. Makes changes to the data management database as required. Generates tracks and resolves data clarifications and queries. Works on assignments that are semi-routine in nature but recognizes the need for occasional deviation from said routine.
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  • Novella Clinical
    Clinical Data Specialist
    Novella Clinical Apr 2015 - Jun 2015
    Morrisville, Nc, Us
    Clinical Data and Query Review: Issue queries and review query responses with the highest level of quality based upon the Data Review Plan, Manual Review (AE/CM compares, Inclusion/Exclusion review, etc.), Aggregate Checks (DM listings), and Reconciliation (LAB, SAE, ECG, and other vendors). Assist with other data reviews for Biostatistics, Medical Review, Sponsor, and other ad hoc reports.
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  • Ppd
    Feasibilty & Site Liaison Associate
    Ppd Jan 2015 - Mar 2015
    Wilmington, Nc, Us
    Represents PPD in the global medical research community. Develops collaborative relationships with investigators and site personnel to conduct feasibility assessments in accordance with feasibility processes and within deliverable timelines. Develops a local knowledge base of sites in the respective market through collaborative working with local PPD personnel. Utilizes local knowledge, PPD systems, external site lists and sponsor directives to develop and review site lists that are suitable for the strategic needs of the feasibility and to provide local input into the site tiering process.
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  • Ppd
    Clinical Data Associate Iii
    Ppd Mar 2012 - Sep 2014
    Wilmington, Nc, Us
    Perform all aspects of the data cleaning process, with minimal supervision, in accordance with Good Clinical Practices and Standard Operating Procedures/Working Practice Documents to assess the safety and efficacy of investigational products. Key responsibilities are data listing reviews, SAE reconciliation, TPV reconciliation, weekly study metrics & UATs.
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  • Inventiv Health Clinical
    Data Analyst
    Inventiv Health Clinical Jan 2012 - Mar 2012
    Raleigh, North Carolina, Us
    Perform data review and query generation Review programmed edit checks Track study progress and issue periodic status reportsParticipate in the completion of all quality control measures necessary for the finalization and transfer of the database and related materials to the sponsor
    View
  • Datatrial
    Study Delivery Associate
    Datatrial Sep 2011 - Dec 2011
    Critically review CRFs as specified in the DMP, raise and track queries, perform data management activities on projects, e.g. tracking, database testing data review and reconciliation, QC.
  • Ppd
    Clinical Data Associate Iii
    Ppd May 2011 - Aug 2011
    Wilmington, Nc, Us
    Discrepancy management activities within OC databases, manual review of data listings, Critical Variables QC & Random Sample QC.
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  • Datatrial
    Study Delivery Associate
    Datatrial Dec 2010 - May 2011
    DM Lead responsible for validating clinical trial data and raising queries to ensure quality and consistency within OC & EDC databases, bi-weekly status updates teleconferences w/sponsor, manual review of data listings, generate/clean reconciliation reports (SAE, Lab), & QC of data for database lock.
  • Health Decisions
    Sr Data Coordinator
    Health Decisions Jan 2007 - Nov 2010
    Morrisville, Nc, Us
    Rreceipt/tracking/scanning of CRFs for data entry, validations, query management, testing of validation rules, & manual review of data listings
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  • Ppd
    Clinical Data Associate Ii
    Ppd Aug 2004 - Jan 2007
    Wilmington, Nc, Us
    Discrepancy Management within the Oracle Clinical database, SAE Reports, Third Party Vendor Reconciliation Reports, & Data Listings Review
    View
  • Ppd
    Clinical Data Analyst
    Ppd Feb 2004 - Jun 2004
    Wilmington, Nc, Us
    Discrepancy Management within the Oracle Clinical database
    View
  • Gsk
    Clinical Data Scientist
    Gsk Jan 2003 - Feb 2004
    Brentford, Middlesex, Gb
    Data Management activities for assigned protocolsCompleteness and consistency of the clinical databaseCommunication & interaction with clinical project teams
    View
  • Inc Research
    Clinical Data Associate
    Inc Research Apr 2002 - May 2002
    Raleigh, North Carolina, Us
    Discrepancy Management within the Oracle Clinical database
    View
  • Kendle International Inc
    Clinical Data Associate
    Kendle International Inc Oct 2001 - Mar 2002
    Raleigh, Nc, Us
    Responsible for reviewing and processing clinical trial data to ensure the accuracy and consistency of the clinical databases.Provided accurately timely and consistent clinical data to both sponsor and other internal strategic business units involving the following data related activities: CRF tracking, data reviewing, validation, query updating.
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  • Pharmaresearch Corporation
    Data Management Associate I
    Pharmaresearch Corporation Aug 2000 - Oct 2001
    Data Management maintenance activities within the ClinTrial database.
  • Duke Clinical Research Institute
    Clinical Data Assistant Ii
    Duke Clinical Research Institute May 2000 - Aug 2000
    Durham, North Carolina, Us
    View
  • Ppd
    Sr Data Entry Operator
    Ppd Aug 1998 - May 2000
    Wilmington, Nc, Us
    View

Eric Hickman Skills

Edc Oracle Clinical Clinical Trials Data Management Cro Inform Clinical Data Management Gcp Medidata Oncology Pharmaceutical Industry Ctms Therapeutic Areas Clinical Development Microsoft Office Protocol Ich Gcp Regulatory Submissions Clinical Research Validation Infectious Diseases Data Entry Cdisc 21 Cfr Part 11 Sas Meddra Sdtm Electronic Data Capture Outlook Clinical Study Design Sop Query Writing Sae Reconciliation Data Validation Clinical Data Microsoft Excel Good Clinical Practice Standard Operating Procedure Cro Management Query Excel Windows Gcps Therapeutic Area

Eric Hickman Education Details

  • North Carolina Central University
    North Carolina Central University
    Accounting
  • New Hanover High School
    New Hanover High School
    College Prep

Frequently Asked Questions about Eric Hickman

What is Eric Hickman's role at the current company?

Eric Hickman's current role is Clinical Data Manager | Data Review, Query Resolution, Reconciliation.

What is Eric Hickman's email address?

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What is Eric Hickman's direct phone number?

Eric Hickman's direct phone number is +191953*****

What schools did Eric Hickman attend?

Eric Hickman attended North Carolina Central University, New Hanover High School.

What skills is Eric Hickman known for?

Eric Hickman has skills like Edc, Oracle Clinical, Clinical Trials, Data Management, Cro, Inform, Clinical Data Management, Gcp, Medidata, Oncology, Pharmaceutical Industry, Ctms.

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