icf

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Senior ICF Medical Writing Project Manager (PM) – 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 last 5 years. As...

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionJoin Us as a Senior ICF Medical Writing Project Manager (PM) – 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 last 5 years. As...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join Us as a Senior ICF Medical Writing Project Manager (PM) – 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 last 5...

Precision Medicine Group in Mexico is seeking a Senior Regulatory and Start Up Specialist to lead country-specific regulatory and site start-up activities for clinical trials. You will manage CTAs, submissions to CA/EC, ICF reviews, essential document handling, and coordination with the Site Contracts team.The role requires deep regulatory experience in...

Precision Medicine Group in Mexico is seeking a Senior Regulatory and Start Up Specialist to lead country-specific regulatory and site start-up activities for clinical trials. You will manage CTAs, submissions to CA/EC, ICF reviews, essential document handling, and coordination with the Site Contracts team.The role requires deep regulatory experience in...

Precision Medicine Group in Mexico is seeking a Senior Regulatory and Start Up Specialist to lead country-specific regulatory and site start-up activities for clinical trials. You will manage CTAs, submissions to CA/EC, ICF reviews, essential document handling, and coordination with the Site Contracts team.The role requires deep regulatory experience in...

ICON Strategic Solutions in Mexico City is seeking a Site Activation Manager to coordinate start-up and activation activities for North American studies. You will build strong sponsor-site relationships, manage essential document collection, and ensure timely regulatory submissions and activation across the US and Canada.The role requires experience in ICH...

ICON Strategic Solutions in Mexico City is seeking a Site Activation Manager to coordinate start-up and activation activities for North American studies. You will build strong sponsor-site relationships, manage essential document collection, and ensure timely regulatory submissions and activation across the US and Canada.The role requires experience in ICH...

Job Overview Under general supervision, perform tasks at a country level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. Essential Functions Under general...

Job Overview Under general supervision, perform tasks at a country level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. Essential Functions Under general...

Job Overview Under general supervision, perform tasks at a country level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. Essential Functions Under general...

Regulatory & Start Up Specialist 1, cFSP Job Overview: The RSU Specialist 1 perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance...

Regulatory & Start Up Specialist 1, cFSPJob Overview:The RSU Specialist 1 perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines.May also include maintenance...

Regulatory & Start Up Specialist 1, cFSP Job Overview: The RSU Specialist 1 perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance...

Un directeur adjoint est en cours de recrutement par le cabinet Citéa Consultants pour la ville de Villemomble. IDF – Au Service De Plus De 31 000 Habitants, Villemomble Est Une Ville Résidentielle Située à Seulement 14 Km à L’est De Paris Reliée à La Capitale Par Le RER E. Membre De L’EPT Grand Paris Grand Est, Cette Commune Met L’accent Sur...

Job OverviewUnder general supervision, perform tasks at a country level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities.Essential Functions• Under general...

Regulatory & Start Up Specialist 1, cFSP Job Overview The RSU Specialist 1 perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance...

Job DescriptionRole Purpose:We are looking for a Clinical Research Support professional to assist with study start-ups, contractsand budgets, patient visit coordination, and ensuring a positive patient experience throughout study participation.This position will provide additional support to the Site Manager, by assisting with day-to-day clinical research...

Do you want to be a part of the world’s leading jewelry company while putting your experience in OTC Accounting into use? If yes, then we might have an exciting opportunity for you! You will be part of Pandora Latin America Team in an international organization of can-do spirited, passionate, and performance-driven people. Pandora is looking for a dynamic...

Job Description Summary WORK ARRANGEMENT: Hybrid Working, #LI-HybridLOCATION: Mexico City, MexicoRELOCATION SUPPORT: This role is based in Mexico City, Mexico. Novartis is unable to offer relocation support: please only apply if accessible. What if your expertise could help accelerate the development of life-changing medicines for patients around the world?...