Global Regulatory Jobs in Fishers, IN

The Associate Director works independently with guidance from a Director and is responsible for developing and implementing the HEOR strategy and tactics supporting more than one indication within the same product or more than one product within the same indication either US or Intern More...

See Yourself at TelixThe Medical Information Lead is a dedicated self-motivated and scientifically driven individual expected to lead Medical Information operations. This key player will serve as the sole person responsible for managing and optimizing daily operations while ensuring a More...

See Yourself at TelixTo support the Groups strategic objectives the Manager GRA Global will oversee Regulatory Affairs for commercial registration activities of PSMA portfolio globally. This role involves conducting regulatory tasks related to new product development securing registra More...

The Associate Director works independently with guidance from a Director and is responsible for developing and implementing the HEOR strategy and tactics supporting more than one indication within the same product or more than one product within the same indication either US or Intern More...

The Director Health Economics & Outcomes Research (OUS) leads the development & execution of projects for on-market and/or pipeline development assets who is the brand/asset leader representing HEOR on cross functional asset/brand teams and in the pipeline commercialization te More...

Sobi is seeking a highly experienced passionate and collaborative Director of Strategic Accounts (DSA) to cover a regional geographic market (NY Metro and surrounding areas) reporting into one of two commercial Strategic Account Leads (East/West). This critical role focuses on the lau More...

The Director Health Economics & Outcomes Research (OUS) leads the development & execution of projects for onmarket and/or pipeline development assets who is the brand/asset leader representing HEOR on cross functional asset/brand teams and in the pipeline commercialization tea More...

The Associate Director works independently with guidance from a Director and is responsible for developing and implementing the HEOR strategy and tactics supporting more than one indication within the same product or more than one product within the same indication either US or Intern More...

The Associate Director Regulatory Affairs US Advertising and Promotion is responsible for setting strategy and leading crossfunctional multidisciplinary therapeutic teams and executes multidivisional initiatives. The Associate Director envisions the future by using global marketplace More...

About This Role:As the Senior Director of Medical Affairs Statistics you will play a pivotal role in leading a dynamic team focused on evidence generation and health technology assessment. This position is critical to ensuring the development and dissemination of scientific evidence o More...

See Yourself at TelixThe Vice President Network Development is responsible for leading the national strategy and execution of contract development and manufacturing (CDMO) activities. This role drives the development of internal drug manufacturing capabilities including process optimi More...

See Yourself at TelixTo support the Groups strategic objectives the Manager GRA Global will oversee Regulatory Affairs for commercial registration activities of PSMA portfolio globally. This role involves conducting regulatory tasks related to new product development securing registra More...

About This Role:As a Senior Medical Director for Alzheimers disease & Dementia (ADD) Clinical Development you will be at the helm of pioneering programs that have the potential to transform lives. Youll lead and oversee clinical development activities across both early and latesta More...

See Yourself at TelixAs the CMC Program Lead you will play a critical role in ensuring successful development and manufacturing of the companys radiopharmaceutical assets. Ensuring the effective of CMC strategies through the cross functional collaboration of internal and external par More...

Job DescriptionJob Summary:We are seeking an experienced and highly motivated Business Analyst with a strong background in Veeva RIM and regulatory publishing processes. The ideal candidate will bring solid business analysis expertise including requirements elicitation documentation a More...

Job DescriptionJob Summary:The Manager (contractor) will be part of Analytical Science and Technology (ASAT) team within Commercial Manufacturing & Supply Chain (CMSC) department. S/He/They will provide support with development and of the analytical CMC strategy by contributing t More...

See Yourself at TelixThe Manager GRA CMC is responsible for managing CMC specific regulatory activities for the development and commercialization of pharmaceutical products. This role requires excellent understanding of technical (Quality/CMC) regulatory requirements guidance the abi More...

See Yourself at TelixThe Global Regulatory Affairs (GRA) Operations Submission Manager is responsible for the management organization and delivery of regulatory submission and submission ready documents at Telix ensuring efficient and compliant document workflows between its departme More...

See Yourself at TelixAs the Director of Pharmaceutical Quality Systems (PQS) you will be a key leader responsible for overseeing and optimizing the comprehensive quality framework that underpins our organizations operations. This strategic role requires a seasoned professional with a More...