Associate Director, Trial Disclosure & Transparency — Hybrid
BioSpace
CSL Behring seeks an Associate Director of Clinical Trial Disclosure and Transparency to lead global disclosure activities across interventional and observational studies. This role drives strategy, implements compliant processes, manages vendor partners, and ensures timely publication of registrations, results, and lay summaries in line with regulatory requirements. The successful candidate will guide cross-functional teams, monitor evolving regulations (FDA, EMA, UK, Canada) and optimize #J-18808-Ljbffr BioSpace
- CSL is seeking an Associate Director, Clinical Trial Disclosure & Transparency to lead our global strategy for public registration, results reporting, and data sharing... ...requirements, and prepare executive updates. This hybrid leadership role suits an experienced disclosure...SuggestedWorldwide
- The Associate Director Clinical Trial Disclosure and Transparency is a global subject matter expert responsible for ensuring timely, accurate, and compliant clinical trial disclosures across all regions and study types (interventional and observational). This role guides...SuggestedWork at officeLocal area3 days per week
- The Associate Director Clinical Trial Disclosure and Transparency is a global subject matter expert responsible for ensuring timely, accurate, and compliant clinical trial disclosures across all regions and study types (interventional and observational). This role guides...SuggestedWork at officeLocal area3 days per week
- CSL Plasma Inc. is seeking an Associate Director for US Patient Advocacy in King of Prussia, PA. This role involves developing advocacy strategies... ...and approximately 7 years of relevant experience. This hybrid role allows for a combination of onsite and remote work schedules...SuggestedRemote work
- CSL Behring is seeking an Associate Director, Project Management to lead the successful operational delivery of global, cross functional R&D... ...role is based in King of Prussia, PA or Maidenhead UK, with a hybrid onsite schedule three days per week. You will report to the TA...Suggested3 days per week
- ...Counsel, Global Clinical Development, as the Associate Director, Senior Counsel, Clinical, you will... ...Clinical Legal Department.This is a hybrid role, requiring three (3) days of onsite... ...include but are not limited to clinical trial research agreements, clinical vendor...Full timePrivate practiceWork at office
$142.4k - $224.1k
...organization. Build and foster close working relationship with clinical trial teams to better understand changing business requirements and... ...No Travel Requirements 10% Flexible Work Arrangements Hybrid Shift 1st - Day Valid Driving License No Hazardous Material(s) No...For contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work€87.75k - €146.25k per year
...and external experts to develop transparent, robust cost-effectiveness, public... ...disease together. Reports to Senior Director, Pharma Modeling Lead This role is hybrid. Expect regular time in the... ...to inform clinical development, trial design and evidence plans. Deliver...Work at officeLocal areaRemote workFlexible hours2 days per week3 days per week$212k - $251k
Position Purpose The Associate Director (AD), Biostatistics, leads the full scope of statistical... ...statistical strategies for the clinical trials and regulatory submissions and is accountable... ...Areas) Work Environment This is a hybrid position with a minimum of 3 days...Interim roleRelocation package- The Opportunity:As the Associate Director, Lead Counsel, Enterprise Contracting Americas (US, Canada... ...process, ensuring alignment, transparency, and mutual benefit for all stakeholders... ...be part of our dynamic team!This is a hybrid role, requiring three (3) days of onsite...Full timeContract workWork at officeFlexible hours
$142.4k - $224.1k
...responsible for managing the end-to-end integrated clinical supply chain across the Company’s Research Laboratories portfolio of clinical trials. GCS oversees the sourcing, labeling, packaging, and global distribution of clinical supplies to clinical sites worldwide.The GCS...Full timeContract workFor contractorsLocal areaWorldwideFlexible hoursShift work$91k - $253.7k
We are seeking an Associate Director, Business Systems to partner closely with Product Managers, Stakeholders and development teams on the Scion Delivery Platform portfolio. This Associate Director will translate stakeholder and client needs into clear, actionable product...Full timeContract workPart timeImmediate startWorldwide- ...that make a meaningful difference worldwide. Could you be our next Associate Director, Medical Affairs (Immunology)? The job is in our King of Prussia, PA or Waltham, MA Office. This is a hybrid position and is onsite three days a week. You will report to the...Work at officeWorldwide3 days per week
$129k - $203.1k
...teams, review and approval of contractor-initiated investigations associated with deviations, negotiation of site and global Technical and... ...: No. Travel Requirements: 25%. Flexible Work Arrangements: Hybrid. Shift: 1st - Day. Valid Driving License: Yes. Hazardous Material...For contractorsRelocationVisa sponsorshipFlexible hoursShift work- ...the Head of US Patient Advocacy & Government Affairs, as the Associate Director, US Patient Advocacy, you will develop and execute key advocacy... ...headquarters or our Washington, D.C. office.This is a hybrid role, which offers a combination of an onsite and remote work...Full timeWork at officeRemote work
$166.5k - $203.5k
...therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a serious liver... ...(F2 to F3). An ongoing Phase 3 outcomes trial is evaluating Rezdiffra for the treatment... ...in the right way.Reporting to the Senior Director, Global Pharmacovigilance Compliance, Standards...Minimum wageFull timeWork at officeLocal areaFlexible hours- The Associate Director, Scheduling and Logisticsleads production scheduling and logistics for all production streams at the Upper Merion... ...necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the...Full timeTemporary workWork at officeLocal area
- CSL is seeking an experienced Associate Director, Senior Counsel, Clinical to provide practical, timely legal support to its... ...manage high-risk, complex agreements like clinical trial and vendor contracts. This hybrid role requires three onsite days weekly and collaboration...
- Harmony Biosciences is recruiting for an Associate Director, Biostatistics in our Plymouth Meeting... ...with the Clinical team on clinical trial design and available statistical methodologies... ...unsolicited and no fee will be payable. Thank you for your cooperation. #LI-HybridWork at officeLocal areaRemote work
- ...therapies that make a meaningful difference worldwide.Could you be our next Associate Director, Project Management? The job is in our King of Prussia, PA or Maidenhead UK office. This is a hybrid position and is onsite three days a week. You will report to TA Portfolio...Full timeWork at officeWorldwide3 days per week
$166.5k - $203.5k
...therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a serious liver... ...(F2 to F3). An ongoing Phase 3 outcomes trial is evaluating Rezdiffra for the treatment... ...the right way. Reporting to the Senior Director, Global Pharmacovigilance Compliance,...Minimum wageFull timeWork at officeLocal areaFlexible hours$129k - $203.1k
The Associate Director, Standards & Execution is responsible for leading the planning, execution... ...effectiveness, and promote transparency across a globally organization. The role... ...Requirements: 10% Flexible Work Arrangements: Hybrid Shift: Not Indicated Valid Driving License...For contractorsLocal areaRelocationVisa sponsorshipFlexible hoursShift work- The Associate Director, Measurement Sciences is a scientific role within Measurement Sciences responsible... ...implemented appropriately in clinical trials. The role requires strong scientific... ...to all federal and state US Transparency requirements. For more information, please...Local areaFlexible hours
$164k - $200.75k
...focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a serious liver disease that can... ...moderate to advanced fibrosis (F2 to F3). An ongoing Phase 3 outcomes trial is evaluating Rezdiffra for the treatment of compensated MASH...Minimum wageFull timeLocal areaFlexible hours$180k - $219k
...therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a serious liver... ...(F2 to F3). An ongoing Phase 3 outcomes trial is evaluating Rezdiffra for the treatment... ...the right way.The Principal / Associate Director Statistical Programmer is an individual...Minimum wageFull timeLocal areaFlexible hours$174.13k - $199.62k
...focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a serious liver disease that can... ...moderate to advanced fibrosis (F2 to F3). An ongoing Phase 3 outcomes trial is evaluating Rezdiffra for the treatment of compensated MASH...Minimum wageFull timeContract workLocal areaFlexible hours- ...About the Role: As a CBRE Associate Property Manager, you will manage a variety of financial... ...disclaimers include U.S. state pay transparency requirements, sponsorship eligibility,... ...requirements, etc. Applicant AI Use Disclosure We value human interaction to...Work at officeVisa sponsorshipFlexible hours
- The Opportunity:Reporting to the Director, Commercial Learning & Development in this newly created Associate Director, Commercial Learning & Development, Market Access... ...support product training as needed.This is a hybrid role, requiring three (3) days of onsite work...Full time
- ...for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at SummaryLocation...Full timeLocal area
$137k - $235.75k
...Innovative Medicine R&D is recruiting for an Associate Director, Regulatory Affairs Labeling Product Leader. This position is a hybrid role and will be located in Raritan, NJ;... ...235,750.00Additional Description for Pay Transparency:Subject to the terms of their respective...Full timeWork experience placementLocal areaImmediate startWorldwide
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