Regulatory Affairs Expert

About LifelancerLifelancer is a talent-hiring platform connecting professionals with opportunities in the Life Sciences, Pharma, and IT domains.Job SummaryWe are seeking a highly skilled Senior Associate Director to lead our global medical affairs learning and training initiatives. This role will drive the development and implementation of comprehensive...

Explore a challenging opportunity as Senior Patient Safety Physician with Boehringer Ingelheim.Job Title: Senior Patient Safety PhysicianLocation: Ridgefield, CT 06877, USA (Remote)Contract Type: Full-timeSeniority Level: Mid-Senior levelDescriptionThe Patient Safety Physician will join our motivated and expert team of physicians in the global Oncology...

Job DescriptionThe Label Development Specialist is accountable for the efficient management of labeling activities, including planning, monitoring, and steering timelines, tasks, and costs. This role ensures timely provision of IMP labels for assigned trials by communicating and negotiating all labeling-related activities within the Global Trial Team.Review...

Job OverviewThe Business Development & Continuity Expert plays a pivotal role in ensuring the Pharmaceutical Development department remains compliant with global regulatory authorities. This involves collaborating cross-functionally with various global partners, establishing suitable systems and training for IMP Delivery employees, and providing advice on...

About Insight GlobalInsight Global is a leading provider of staffing and business solutions. Our team of experts helps clients find top talent to drive their business forward.Job DescriptionWe are seeking a Senior Pharmaceutical Development Expert to join our team. As a key member of our client's Pharmaceutical Development department, you will play a...

Company OverviewYoh, A Day & Zimmermann Company, is a leading global staffing firm with a presence in over 150 worldwide locations. Founded in 1940, Yoh operates from 75 locations throughout North America and is headquartered in Philadelphia, PA.Job SummaryWe are seeking an experienced Business Development & Continuity Expert to join our team in Ridgefield,...

About the RoleWe are seeking a highly skilled Clinical Safety Physician Lead to join our team at BioCT Innovation Commons. In this role, you will be responsible for leading pharmacovigilance risk management activities on a global level.As a key member of our team, you will develop proactive risk management strategies for assigned marketed and/or...

OverviewWe are seeking a highly skilled Clinical Data Science Expert to support our pharmaceutical research efforts. This role will play a critical part in the development of new treatments and therapies.About UsLifelancer is a leading talent-hiring platform in Life Sciences, Pharma, and IT. We connect talented individuals with opportunities in pharma,...

Job Title: Clinical Trials Labeling SpecialistAbout Nesco ResourceNesco Resource is a leading provider of clinical trial solutions, dedicated to delivering high-quality services to our clients.Estimated Salary: $70,000 - $90,000 per yearJob DescriptionAbout the Role:We are seeking an experienced Clinical Trials Labeling Specialist to join our team. In this...

The position of Medical Director, Clinical Risk Management Lead, is a critical role within BioCT Innovation Commons. The ideal candidate will have a strong medical background, with a minimum of 5 years of experience in the pharmaceutical industry, preferably in pharmacovigilance.Job Description:This senior-level position requires a US MD or DO degree or...

Job DescriptionWe are seeking a highly skilled Senior Label Development Specialist to join our team at Nesco Resource.About the RoleThis is a key position in our organization, responsible for processing, planning, and steering timelines, tasks, and costs for labeling activities performed at internal or external vendors supporting global clinical trials phase...

About the RoleWe are seeking an experienced Business Development & Continuity Expert to join our team at Maxis Clinical Sciences. The successful candidate will be responsible for ensuring the Pharmaceutical Development department remains compliant with global regulatory authorities.The ideal candidate will have a strong background in business development,...

Job OverviewThis Senior Clinical Trial Manager role offers a unique opportunity to join a leading company in the clinical research industry. As a key member of our team, you will be responsible for overseeing the execution of monitoring plans and ensuring the quality of monitoring performed by CRAs for assigned US conducted trials.Key ResponsibilitiesDevelop...

About the CompanyMaxis Clinical Sciences is a leading provider of complete solutions for clinical and digital services. With a global presence across three continents, we offer 24/7 delivery and operate with a problem-solving approach that prioritizes genuine relationships and steady communication.About the RoleThe Senior Clinical Trial Manager will join our...

DescriptionDo you have a knack for strategic planning and global operations management? Do you thrive in dynamic, cross-functional environments and have a passion for making a difference in the healthcare landscape? As the Global Capability Owner (GCO) for Non-Trial Activities (NTAs), you will play a pivotal role in shaping the future of our capabilities in...

Business Development & Continuity Expert - Program Manager II Ridgefield CT, 06877, Hybrid schedule 2 YearsDuties: The Business Development & Continuity Expert represents the Pharmaceutical Development department in audits and inspections by global regulatory authorities, collaborating cross-functionally with various global partners. They independently...

Business Development & Continuity Expert - Program Manager II Ridgefield CT, 06877, Hybrid schedule 2 YearsDuties: The Business Development & Continuity Expert represents the Pharmaceutical Development department in audits and inspections by global regulatory authorities, collaborating cross-functionally with various global partners. They independently...

Job title: Business Development & Continuity Expert Location: Ridgefield CT, 06877 Duration: 2 yearsNumber of Positions: 1 Duties: The Business Development & Continuity Expert represents the Pharmaceutical Development department in audits and inspections by global regulatory authorities, collaborating cross-functionally with various global partners. They...

Job Name: Business Development & Continuity ExpertLocation: Ridgefield, CTType: Contract Overview Join one of the largest pharmaceutical that is driven by science and seek to push the boundaries of what's possible in medicine and explore new options in life-enhancing treatments. Responsibilities The Business Development & Continuity Expert represents the...

Business Development & Continuity Expert - Program Manager II Ridgefield CT, 06877, Hybrid schedule 2 Years Duties: The Business Development & Continuity Expert represents the Pharmaceutical Development department in audits and inspections by global regulatory authorities, collaborating cross-functionally with various global partners. They independently...

Business Development & Continuity Expert - Program Manager II Ridgefield CT, 06877, Hybrid schedule 2 Years Duties: The Business Development & Continuity Expert represents the Pharmaceutical Development department in audits and inspections by global regulatory authorities, collaborating cross-functionally with various global partners. They independently...

Business Development & Continuity Expert - Program Manager II Ridgefield CT, 06877, Hybrid schedule 2 Years Duties: The Business Development & Continuity Expert represents the Pharmaceutical Development department in audits and inspections by global regulatory authorities, collaborating cross-functionally with various global partners. They independently...

The Director has responsibility for pharmacovigilance risk management activities of marketed and/or investigational compounds on a global level. This may include a portfolio of products/investigational compounds within an assigned disease area or TA. In addition to reporting to US line management, this position may matrix report into a Head Risk Management...

The Director has responsibility for pharmacovigilance risk management activities of marketed and/or investigational compounds on a global level. This may include a portfolio of products/investigational compounds within an assigned disease area or TA. In addition to reporting to US line management, this position may matrix report into a Head Risk Management...

Title: Label Development Specialist Duration: 12 Months (Possible Extension) Location: Hybrid - Ridgefield CT (06877) Duties: The Label Development Specialist is accountable for processing, planning, monitoring, and steering of timelines, tasks and costs for labeling activities performed at internal or at the packaging & labeling vendor supporting global...

Title: Label Development Specialist Duration: 12 Months (Possible Extension) Location: Hybrid - Ridgefield CT (06877) Duties: The Label Development Specialist is accountable for processing, planning, monitoring, and steering of timelines, tasks and costs for labeling activities performed at internal or at the packaging & labeling vendor supporting global...

Duties:The Label Development Specialist is accountable for processing, planning, monitoring and steering of timelines, tasks and costs for labeling activities performed at internal or at the packaging & labeling vendor supporting global clinical trials phase I – IV. The Label Development Specialist ensures within the Global Trial Team the timely provision...

Duties:The Label Development Specialist is accountable for processing, planning, monitoring and steering of timelines, tasks and costs for labeling activities performed at internal or at the packaging & labeling vendor supporting global clinical trials phase I – IV. The Label Development Specialist ensures within the Global Trial Team the timely provision...

Duties:The Label Development Specialist is accountable for processing, planning, monitoring and steering of timelines, tasks and costs for labeling activities performed at internal or at the packaging & labeling vendor supporting global clinical trials phase I – IV. The Label Development Specialist ensures within the Global Trial Team the timely provision...

Duties:The Label Development Specialist is accountable for processing, planning, monitoring and steering of timelines, tasks and costs for labeling activities performed at internal or at the packaging & labeling vendor supporting global clinical trials phase I – IV. The Label Development Specialist ensures within the Global Trial Team the timely provision...

Job DescriptionJob DescriptionA large pharmaceutical client in Ridgefield, CT is looking for a Business Development & Continuity Expert to sit hybrid 2-3 days a week onsite. The Business Development & Continuity Expert represents the Pharmaceutical Development department in audits and inspections by global regulatory authorities, collaborating...

Job DescriptionJob DescriptionA large pharmaceutical client in Ridgefield, CT is looking for a Business Development & Continuity Expert to sit hybrid 2-3 days a week onsite. The Business Development & Continuity Expert represents the Pharmaceutical Development department in audits and inspections by global regulatory authorities, collaborating...

The Business Development & Continuity Expert represents the Pharmaceutical Development department in audits and inspections by global regulatory authorities, collaborating cross-functionally with various global partners. They independently establish suitable systems and training for all IMP Delivery employees and team leaders, providing advice on compliance...

Title: Label Development Specialist Duration: 12 Months (Possible Extension)Location: Hybrid - Ridgefield CT (06877) Duties: The Label Development Specialist is accountable for processing, planning, monitoring, and steering of timelines, tasks and costs for labeling activities performed at internal or at the packaging & labeling vendor supporting global...