Clinical Development Jobs in Houston, MS

This Position is Contingent Upon Award of the Contract. Under the direction of the National Program Director and in collaboration with the Office of the Chief Medical Officer (OCMO) of U.S. Customs and Border Protection (CBP) the National Medical Director (NMD) and the Deputy Nat More...

This Position is Contingent Upon Contract Award.Under the direction of the National Program Director and in collaboration with the Office of the Chief Medical Officer (OCMO) of U.S. Customs and Border Protection (CBP) the National Medical Director (NMD) and the Deputy National Medical More...

This Position is Contingent Upon Award of the Contract.   The Medical Director is responsible for medical oversight direction and leadership of the medical staff regarding all areas of healthcare for the project.  The Medical Director scope of work to provide direc More...

About This Role We are seeking a dynamic and experienced Associate Director Field Medical Training & Excellence Global Medical Affairs to enhance the performance and capabilities of our Field Medical teams worldwide. This critical role integrates therapy area expertise Field Medi More...

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and wellbeing.HomeBased in the United StatesResponsibilities:Advise clients project teams sites data safety monitoring boards More...

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and wellbeing.HomeBased in USResponsibilities:Advise clients project teams sites data safety monitoring boards regulatory agen More...

The TA Lead Global Rheumatology Pipeline leads a team in a therapeutic area in developing and executing the Medical Affairs strategy for an AbbVie asset in development or a market product.  Responsible for practical and clinically meaningful data strategy and delivery to inf More...

(The role requires weekly to cover PST time for a couple of days) The Scientific Affairs Manager (SAM) is responsible to inform engage and influence key stakeholders (KSH) at strategic pharma and biotech companies regarding scientific and clinical data supporting Guardant Health More...

About This Role:Pharmacometric analyses and insight are critical in the development of drug candidates determination of product viability and maximization of commercial value at Biogen. The Associate Director Pharmacometrics has responsibility for high priority clinical development as More...

About This RolePharmacometric analyses and insight are critical in the development of drug candidates determination of product viability and maximization of commercial value at Biogen.  As the Director Pharmacometrics you have responsibility for high priority clinical development More...

At Adtalem Global Education we are committed to empowering students and transforming lives through education. As a Senior Regulatory Affairs Analyst you will play a critical role in ensuring compliance with federal state and accreditor regulations helping to shape policies and process More...

Vice President Regulatory AffairsHybrid/Remote Options AvailableAre you a strategic leader with a passion for regulatory compliance and higher education Join our team as Vice President of Regulatory Affairs where you will shape compliance strategies build key regulatory relationships More...

Job Title: Regional Regulatory Manager Job Location: Houston TX USA Job Location Type: Remote Job Contract Type: Fulltime Job Seniority Level: MidSenior level A Place Where People Matter. Start your career journey with Univar Solutions! Here you can make an impact on the world around More...

About This RoleAs a Senior Manager Aggregate Report Scientist you will be an integral part of the Safety Surveillance and Aggregate (SSA) Reports team. In this pivotal role you will oversee the pharmacovigilance processes for all aggregate reports including PSURs DSURs PADERs and loca More...

At Adtalem Global Education we are committed to empowering students and transforming lives through education. As a Senior Regulatory Affairs Analyst you will play a critical role in ensuring compliance with federal state and accreditor regulations helping to shape policies and process More...

About This RoleBiogens Decision & Quality Analytics Innovation (DQAI) team part of Portfolio Leadership Analytics & Insights (PLAI) under Research Development and Medical (RD&M) leverages advanced analytics to provide strategic insights and prescriptive recommendations for More...

About This RoleAs a Senior Manager Aggregate Report Scientist you will be an integral part of the Safety Surveillance and Aggregate (SSA) Reports team. In this pivotal role you will oversee the pharmacovigilance processes for all aggregate reports including PSURs DSURs PADERs and loca More...

Advising clients on compliance with the Securities Act Securities Exchange Act Advisers Act and other applicable regulatory directives with little input from senior team members.Advising on and reviewing firm marketing and advertising materials for compliance with the Advisers Act and More...

About This Role Leading and taking full accountability in the successful creation ownership and execution of US Medical Affairs (USMA) operational processes and activities the Sr Manager Medical Affairs Operations Lead (specialty Care) is a critical member of the US Medical Affairs te More...

The Manager Regulatory Affairs US Advertising & Promotion combines knowledge of scientific regulatory and business issues to enable products that are developed manufactured or distributed to meet required legislation. Has responsibility for 12 of the following: therapeutic area pr More...