Clinical Trial Specialist
On Assignment, Inc./Oxford Global Resources

Scottsdale, Arizona


Summary:

Responsible for developing and managing all aspects of the global clinical study data management process from start-up to database lock and regulatory submission support

Project Details:

* Coordinate activities with the internal and external BioStats, laboratory vendors, database programming and trial operations to define and implement data management requirements
* Ability to develop and own processes related to data compilation, tracking, maintenance, cleaning, and finalization including the ability to develop, run, review, and maintain data listings for laboratory and database data
* Flag findings during ongoing study to clinical management and may develop materials and present to CRAs, sites to ensure consistent, quality data capture
* Facilitate and lead all data cleaning including issuing queries along with guidance on issuance and acceptable closure of queries on an ongoing basis
* Demonstrate a strong understanding of the assigned study protocol(s), critical tasks, and associated milestones
* Ensure completeness, correctness and consistency of routine clinical data and its structure
* Weekly reconciliation with multiple vendors to ensure timely and quality data entry, lab completion and resulting, and eDiary data entry and compliance
* Work closely with DM CRO to ensure all eCRFs, CCGs, Edit Checks, SOPs and DMPs meet study requirements and assist with updates as required
* Assistance with any required updates to the EDC system and associated UAT, and updated documentation
* Work collaboratively with both internal team members and associated CROs / vendors to meet project deliverables and timelines for clinical data acquisition, quality review, clinical study reports, documents required for regulatory submission and assistance as needed
* Close collaboration with Stats and Clinical teams to manage frequent DMC meetings including timeline development, data cleaning, management of EDC and lab data transfers, and more
* Aid study manager in managing and tracking database interim review and lock timelines and ensure CDM project milestones are met in coordination with the project team
* Develop and maintain relevant report metrics to share with overall study team and upper management
* The ability to note and monitor trends across regions will be key
* Support study-level audit and inspection readiness activities, as needed

Job Experience:

* Minimum of 5 years DM experience with at least two years at a Sponsor company
* Experience and familiarity with global Phase 2 and 3 trials
* Experience and familiarity with interim analyses, and freezing and locking databases
* Excellent communication and time management skills
* Ability to prioritize study load and associated tasks
* Chosen candidate must be autonomous, independent and must take initiative to manage, own, and lead all aspects of DM while contributing to overall study team

Oxford is an Equal Employment Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law. Oxford will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. Oxford is committed to working with and providing reasonable accommodation to individuals with physical and mental disabilities. If you need special assistance or an accommodation while seeking employment, please email oxfordbenefits@oxfordcorp.com. We will make a determination on your request for reasonable accommodation on a case-by-case basis.



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