Global Senior Director of Medical Affairs, Prostate Cancer

Job Summary:The Global Senior Director Medical Affairs (GDMA), Oncology is a key member of the Product Development Team and Global Human Health commercialization teams. They are responsible for driving execution of scientific & medical affairs plans for the assigned therapeutic area (Prostate Cancer) in key countries and regions.Key Responsibilities:Develop...

**Become a Key Player as a Lead CMC Regulatory Affairs Specialist** Insight Global is in search of a committed professional to join the Global Regulatory Affairs division of a leading pharmaceutical organization. **Key Responsibilities Include:** Crafting comprehensive CMC regulatory approaches Preparing a variety of regulatory CMC documents including...

Job DescriptionJob SummaryWe are seeking a highly skilled and experienced Regulatory Affairs Director to join our team at MSD Malaysia. As a key member of our Regulatory Affairs Department, you will be responsible for managing a team of Regulatory Affairs Specialists and ensuring the smooth operation of all registration activities across the teams defined...

Job SummaryThe Executive Director, Policy Development and Strategy will lead the development and implementation of global policy strategies to drive business growth and mitigate risks. This role will be responsible for monitoring policy and geopolitical trends, directing policy development activities, and facilitating proactive engagement on cross-cutting...

About the RoleThe Pharma Documentation Specialist will support the operational aspects of procedural documentation management and advise on documentation strategy for Global Regulatory Affairs & Clinical Safety (GRACS) organization within Research Laboratories (MRL).Key ResponsibilitiesSupport and manage the creation/revision of Regulatory Affairs and Global...

Job DescriptionCollabera is seeking a highly skilled Pharma Documentation Specialist to join our team.About the Role:The successful candidate will support the operational aspects of procedural documentation management and advise on documentation strategy for Global Regulatory Affairs & Clinical Safety (GRACS) organization within Research Laboratories...

Job Description**Job Summary**We are seeking a highly skilled Regional Market Access Associate Director to join our Oncology team in MSD Malaysia. The successful candidate will be responsible for developing and implementing comprehensive patient access strategies for Oncology therapies in the Latin America region.Key ResponsibilitiesDevelop and Implement...

Job DescriptionJob SummaryWe are seeking a highly skilled and experienced Regulatory Affairs Director to join our team at MSD Malaysia. The successful candidate will be responsible for managing a team of Regulatory Affairs Specialists and ensuring the smooth operation of all registration activities across the teams defined responsibilities.Key...

Job Title: Senior Documentation SpecialistAt Spectraforce Technologies, we are seeking a highly skilled Senior Documentation Specialist to join our team. As a key member of our Global Regulatory Affairs & Clinical Safety (GRACS) organization, you will be responsible for supporting the operational aspects of procedural documentation management and advising on...

Job DescriptionJob Title: Senior Principal Scientist, Breast CancerCompany: MSD MalaysiaJob Summary:We are seeking a highly experienced and skilled Senior Principal Scientist to join our team in Breast Cancer Research. The successful candidate will be responsible for leading clinical research activities, developing clinical development strategies, and...

Key Responsibilities and Qualifications: Independently contribute to new product development teams by formulating regulatory strategies and preparing necessary documentation for both domestic and international submissions concerning IVD medical devices, emphasizing instrumentation and software/hardware, alongside experience in assay development. Proven...

Key Responsibilities and Qualifications: Independently assist core teams in the development of new products by formulating regulatory strategies and preparing necessary documentation for both domestic and international submissions related to IVD medical devices, emphasizing instrumentation and software/hardware, along with experience in assay development....

Job Title: Scientific Project Coordinator Job Location: Rahway, NJ and Upper Gwynedd, PA Job Duration: 12 months+ Pay Range: $55 - $61.87/hr on W2 Shift: Hybrid role - 3 days onsite required each week. Job Overview: We are in search of a proactive and innovative Scientific Project Coordinator who will play a pivotal role in steering our Strategic...

Senior Principal Scientist/Senior Director, Precision BioinformaticsMSD Malaysia is seeking a highly experienced computational biologist to lead our Companion Diagnostics (CDx) efforts in San Diego.Job Summary:We are looking for a senior leader to oversee the development of a flexible AI/ML engine for precision bioinformatics, leveraging human data to...

Position: Marketing Project ManagerLocation: RemoteContract Duration: 12 Months with Potential for ExtensionCompensation: $45/hr on W2Essential Qualifications:Experience in Marketing Product Launch3-5 years in Project/Program ManagementBackground in the Pharmaceutical SectorExperience in OncologyRole Overview:• Facilitate strong collaboration among global,...

Position OverviewDPS Group is seeking a qualified BioPharma Senior Process Project Engineer to oversee equipment commissioning, calibration activities, and documentation within a GMP environment. The successful candidate will possess the necessary skills and technical expertise to support project timelines, documentation, facilities, and vendor resources,...

Job SummaryWe are seeking an experienced Health, Safety, and Environment Director to join our team at ESR Healthcare. As a key member of our organization, you will play a critical role in driving our safety culture, developing our HSE strategy, and ensuring compliance with regulatory requirements.Key Responsibilities:Lead and manage the development and...

Job Title: Documentation SpecialistJoin eTeam as a Documentation Specialist and take on a challenging role that requires strong organizational and communication skills. As a key member of our team, you will be responsible for supporting the operational aspects of procedural documentation management and advising on documentation strategy for our client's...

Job SummaryWe are seeking a highly experienced and skilled Senior Leadership Position - Managing Director Saudi Arabia to lead our business in Saudi Arabia. As a key member of our GCC Cluster leadership team, you will be responsible for driving business growth, developing and executing strategic plans, and leading cross-functional teams to achieve business...

Job SummaryWe are seeking a skilled Documentation Management Specialist to join our team at Intelliswift. In this role, you will be responsible for supporting the operational aspects of procedural documentation management and advising on documentation strategy for our Global Regulatory Affairs & Clinical Safety (GRACS) organization.Key...