Director of Clinical Affairs - Trials & KOL Strategy Lead
Socket.dev
Ceribell is seeking a Director of Clinical Affairs to define and execute the clinical evidence strategy for new products. You will plan and manage clinical trials, interact with KOLs, and ensure investigations meet regulatory standards and align with business goals. The role requires leadership across Regulatory, R&D and Go-to-Market, overseeing protocols, data interpretation and publications while maintaining high ethical standards. Competitive compensation and comprehensive benefits offered. #J-18808-Ljbffr Socket.dev
- Ceribell, Inc. is seeking a Director of Clinical Affairs to define and execute the clinical evidence strategy for the Ceribell System. This hybrid role in Sunnyvale will lead trial design, regulatory submissions, and KOL collaborations to drive product validation and market...Suggested
$208k - $256k
...Position Overview:The Director of Clinical Affairs will specifically... ...the clinical evidence strategy supporting new products... ...execution of clinical trials aligned with company... ...leaders in the field (KOLs) and managing the... ...and commercial goals.Lead the planning, design...SuggestedLocal areaShift work- ...DescriptionPrimary Function of PositionThe Director, Clinical Affairs- Endoluminal will guide, develop and execute long range clinical trial strategies, inclusive of first human use,... ...indicationsRoles and ResponsibilitiesPlay a lead role in the development of the company’...SuggestedLocal areaWorldwideFlexible hours
$200k - $230k
Position: Sr. Director, Clinical Affairs Location: Los Gatos, CA Job... ...IDE pivotal clinical trial. This individual will... ...key opinion leaders (KOLs). Responsibilities,... ...Develop and propose strategies to address study issues... ...informed consent documents; lead content and...SuggestedFull timeTemporary workFor contractorsWork experience placement- Intuitive is seeking a Director of Clinical Affairs for Endoluminal to lead long-range clinical trial strategies, including first human use and post‑market evidence generation. The role requires global collaboration with R&D, Regulatory, and GPA to optimize evidence plans...Suggested
- Google's Regulatory Affairs team seeks a seasoned program manager to lead a cross-functional group across legal, product, and regulatory functions, driving strategy for complex matters including litigation and regulatory inquiries. You will develop PM methodologies, mentor...Flexible hours
- Google is seeking a Manager of Regulatory Affairs within the Regulatory PMO, based in Mountain View, CA. The role focuses on owning outcomes, guiding decisions, and influencing stakeholders across global regulatory initiatives. Requirements include a Bachelor's degree and...
- Supira Medical, a clinical-stage Shifamed portfolio company, seeks a Sr. Director, Clinical Affairs to own the IDE pivotal trial from site activation to database lock. You will partner with... ...Marketing, managing CROs, sites, and KOLs to ensure on-time, within-budget...
- ...evidence generation strategy and execution of clinical studies. The Senior... ...member of the Clinical Affairs team, this role will... ...(CRAs), clinical trial assistants (CTAs) and... ...DutiesResponsible for leading assigned clinical... ..., investigators and KOLs to develop and review...Interim roleLocal areaRemote workWorldwideFlexible hoursShift work
- ...evidence generation strategy and execution of clinical studies. The Senior... ...member of the Clinical Affairs team, this role will... ...(CRAs), clinical trial assistants (CTAs) and... ...Duties Responsible for leading assigned clinical... ..., investigators and KOLs to develop and review...Interim roleRemote work
$170 - $180 per hour
...President, Medical Director - Bayside... ...and executing the clinical strategy, from early-stage... ...monitor clinical trials (Phase 1-3) for oncology... ...and Interpretation: Lead medical review, analysis... ..., regulatory affairs, biostatistics, data... ...opinion leaders (KOLs), investigators, and...Full time- Roche seeks a dynamic Endocrinology and Fertility Subchapter Lead within the Medical Value Assays Regulatory Affairs Leadership Team to guide strategy and cross‑functional collaboration in Roche Diagnostics’ regulatory capabilities. You will coach 10-15 staff, manage resources...
$109k - $174.8k
...merit. Job Function Regulatory Affairs Group Job Sub Function... ...Senior Regulatory Affairs Program Lead to support our... ...candidate will lead regulatory strategy development and execution for... ...exceptional engineering and clinical teams, supporting product development...Local areaImmediate startRemote work- Apple Inc. is seeking a Principal Regulatory Affairs Associate in Cupertino, CA, to lead regulatory strategy for medical devices and SaMD products. This hybrid, in-person role will drive submissions and regulatory plans for US and global markets. The successful candidate...
- Intuitive in Sunnyvale, CA seeks an experienced Regulatory Affairs professional to provide expert leadership in global submissions and compliance strategy. The role focuses on cross-functional coordination, technical documentation, and agency interactions to support product...Worldwide
- Kelly Services seeks a Sr Regulatory Affairs Specialist to lead regulatory reporting assessments for manufacturing, facility, product, and packaging... ...with regulators during audits, and guide compliance strategies in a remote, 1-year contract role. The position requires deep...Remote jobContract work
- Johnson & Johnson Innovative Medicine is seeking a Senior Regulatory Affairs Program Lead to guide regulatory strategy for OTTAVA robotic instruments and accessories. You will work with engineering and clinical teams to drive submissions and health authority communications....Remote job
- Intuitive Surgical, Inc. in Sunnyvale seeks a principal‑level Regulatory Affairs professional to lead regulatory strategy across robotic platforms, instruments, disposables, and software. You will shape submission and lifecycle strategies from design through post‑market...Worldwide
- Johnson & Johnson is seeking a Senior Regulatory Affairs Program Lead to support the OTTAVA robotics group, focusing on regulatory strategy for robotic instruments and accessories. You will collaborate with engineering and clinical teams to develop submissions, drive global...
$215k - $255k
...Alto Neuroscience is seeking a Director, Clinical Development to add to our Clinical Trials team. This role plays a key role... ...operations, regulatory affairs, and other departments to support... ...medical input into risk management strategies.Assess and contribute to the development...Local areaRemote work- ...Lead Biostatistician (Finance) Company Description... ...leader within the Clinical Affairs department, the Lead Biostatistician... ...pivotal pre-market trials and post-market... .../or interim analysis strategy. Serve as the final internal... ...Key Opinion Leaders (KOLs), and external...Interim roleWork at officeLocal areaRemote workWorldwideRelocationFlexible hoursShift work
$300k - $309k
...movement! The Medical Director will be a key member... ...support Ceribell's strategy to expand clinical indications, develop... ...and implement clinical trials to continue to build... ...Will Do Strategy Lead medical strategy and... ...Identify and develop KOL and physician...Local areaRemote workFlexible hours2 days per week$151k - $178k
Title: Lead Regulatory Affairs Specialist This position is based in our Campbell, California offices... ...effective regulatory assessments, strategies, documents, and other project deliverables... ...related to bench, animal, and human clinical test plans, reviewing and approving...Full timeWork experience placementShift work$160k - $253k
...factories. We are looking for a Senior Technical Marketing Engineer to lead and develop technical content for DSX. Want to create and tell... ..., customers, and the NVIDIA field.Convert the narrative strategy into consistent and complete technical content across the portfolio...Full time- ...own the components for our HPC compute systems. You will define end-to-end strategy for CPUs, memory, power stages, and related parts, coordinating with hardware engineering and suppliers. Lead supplier negotiations, capacity planning, and lifecycle management; build should...
- System One is seeking a Sr. Regulatory Affairs Specialist in Sunnyvale, CA. The role requires a BS degree and at least 8 years of Regulatory Affairs experience in medical devices. You will lead regulatory plans, prepare FDA 510(k) submissions, and guide product teams on...
$142k - $192.5k
...reporting integrity and readiness for change. Within SRCO, the SOX Strategy, Operations & Audit Excellence team is responsible for end-to-... ...areas including AI governance. Role Summary We're looking for a Lead, SOX Program Strategy & Audit Excellence who thrives at the...Work experience placementWork at office- Intuit is expanding its Consumer Lending focus and seeks a Senior Credit Risk Analyst to lead data-driven risk strategies across the consumer banking portfolio. You will partner with product, data science, compliance, and risk teams to build scalable risk solutions, improve...
$152k - $206k
Intuit Inc. is seeking a Lead, SOX Program Strategy & Audit Excellence in Mountain View. This role demands extensive expertise in risk management and technology governance, focusing on automated and AI-related controls. The ideal candidate will collaborate closely with...- Intuit is seeking a Lead, SOX Program Strategy & Audit Excellence to bridge risk management, audit execution, and technology. You will own AI SOX governance and IT general controls, coordinating with Finance, Accounting and Tech stakeholders to ensure strong financial...
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