- ICON Clinical Research (North Wales, PA)
- TMF Specialist is to perform all duties related to the timely processing of essential and non-essential clinical trial documents to facilitate study startup, ... drug shipment, eTMF maintenance and support eTMF inspection readiness activities **This role is located in North Wales, PA. 5 days onsite to start. Will become hybrid at some point.** **EXPERIENCE & SKILLS** + Ability to interact with Clinical and Regulatory… more
- BeiGene (San Mateo, CA)
- …Regional Clinical Study Manager and the Global Study Management Associate. + Supports the TMF specialist with country/site level TMF creation and maintains ... visit preparations, equipment management, Contract support, EC/regulatory submission preparation/tracking, TMF filing, SUSAR submission, etc. Timelines, Planning and Execution… more
- BeiGene (Emeryville, CA)
- **General Description:** Responsible for managing all TMF operations and is accountable for TMF quality, inspection readiness, and compliance. Provides Trial ... Master File ( TMF ) related assistance to study teams. Involved in TMF management process generation and optimization, including but not limited to the draft and… more
- Randstad US (San Rafael, CA)
- study specialist ii. + san rafael , california + posted 2 days ago **job details** summary + $38.51 - $45.31 per hour + contract + bachelor degree + category life, ... hour work hours: 9 to 5 education: Bachelors responsibilities: Role Summary The Study Specialist II (SS-II) contributes to or leads tasks related to the oversight of… more
- Randstad US (North Chicago, IL)
- clinical documentation specialist ii. + north chicago , illinois (remote) + posted 8 days ago **job details** summary + $38.31 - $45.22 per hour + contract + ... Management Systems preferred. skills: GCP (Good Clinical Practice), ICH Regulations, TMF Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation,… more
- Regeneron Pharmaceuticals (Armonk, NY)
- The Clinical Study Specialist (CSS) provides technical and administrative support to the clinical study team(s) responsible for clinical trial execution. The CSS may ... registry postings + Performs scheduled reconciliations of study Trial Master File ( TMF ) with clinical study lead guidance + Ensures scheduled reports are received… more
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