Senior Director, Scientific Strategy - Wilmington, NC

The Science Lead supports PCR business planning, solution development and delivery, and reputation through developing and implementing a scientific strategy that maintains our reputation as thought leaders. · ...

We are seeking a Senior Director to lead our scientific strategy team. This role will oversee senior scientists and junior staff to deliver high-quality science projects. · Develop and implement scientific strategy to maintain our reputation as thought leaders. · Publish annual s ...

The Senior Director will oversee PCR's scientific strategy and lead cross-functional teams. They will develop an annual scientific strategy statement and coordinate response to industry initiatives. · The role requires a PhD in health outcomes and patient-centered research with s ...

Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. · ...

This is a fully remote position that requires a recognized expert in Clinical Outcome Assessments (COA) strategy with high external visibility and strong track record of publications and presentations. The role involves maintaining an established line of research and providing se ...

The Vice President of Project Delivery will lead the growth strategy for the vaccines book of business at PPD/CRG. · Advanced degree in a relevant scientific discipline. · Detailed knowledge of vaccines development and delivery environments. · Prior experience in leadership roles ...

+Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. · ...

Patient First optimizes patient recruitment and engagement, site operations, and quality data collection. · Lead multiple global studies. · Implement strategy/drive delivery using recruitment and retention tools. · Collaborate with Enrollment Vendor Leads to avoid redundancy of v ...

We are looking for a Principal Medical Writer to join our team at Thermo Fisher Scientific. As a key member of our Medical Writing team, you will be responsible for crafting high-quality medical and scientific writing from planning and coordination through delivery of final draft ...

As part of the Thermo Fisher Scientific team you'll discover meaningful work that makes a positive impact on a global scale.Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier cleaner and safer.Bachelor's degree ...

At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. · ...

As Medical Science Liaison, Neuromuscular you will serve as an externally facing scientific partner that transforms medical practice and shapes the healthcare ecosystem using a data-driven AI-enabled approach to deliver personalized scientific engagement to Healthcare Organizatio ...

We are excited to announce that we are looking for an FSP Medical Writing Manager in the United States Are you an experienced Medical Writer ready to take the next step in your career? Do you thrive leading teams and driving excellence in clinical documentation? · We are looking ...

Pharma Services Group at Thermo Fisher Scientific is a leading contract development and manufacturing organization offering end-to-end services for drug development clinical trial logistics and commercial manufacturing. · ...

The Director Regulatory Affairs provides operational leadership for the department, overseeing innovative solutions including regulatory expertise and client interface to provide strategic regulatory intelligence and guidance for product development from preclinical through regis ...

Lensa is a career site that helps job seekers find great jobs in the US. We are not a staffing firm or agency. · Lead or support study operational strategy and planning and oversee execution of select clinical studies (global/regional and/or local country) for assigned clinical p ...

The job involves leading or supporting the operational strategy and planning for clinical studies. The successful candidate will oversee execution of select clinical studies in compliance with quality standards on schedule and on budget. · ...

Join Us as a Country Approval Specialist (Site Activation Specialist)- Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning · 2,700 clinical trials across · 100+ countries in the la ...

The Regulatory Intelligence Manager will play a pivotal role in monitoring, analyzing and communicating global regulatory developments that impact the client's pipeline and operations. · ...

Manages experienced professionals and / or subordinate management who exercise latitude and independence in their assignments. Often heads one or more sections or a small department. · Bachelor's degree or equivalent and relevant formal academic / vocational qualification · ...