Phaidon International
About Phaidon International

Jump to Austria | Belgium | Canada | Croatia | Europe | France | Germany | Switzerland | US- | US-AZ | US-CA | US-CO | US-CT | US-DC | US-DE | US-E | US-FL | US-IL | US-IN | US-KY | US-LA | US-MA | US-MD | US-MO | US-N | US-NC | US-NH | US-NJ | US-NV | US-NY | US-Nationwide | US-OH | US-PA | US-S | US-SC | US-TX | US-WV

Austria Back to Top
Austria, QA Specialist - Austria
Austria, Quality Assurance Manager - Medical Device - Austria
Belgium Back to Top
Belgium, Interim Qualified Person - Belgium
Belgium, Quality Assurance Manager Opportunity - Belgium - Leading global pharma company
Belgium, Senior MSL - Belgium
Belgium, Senior MSL - Belgium
Canada Back to Top
Canada, Clinical Research Project Manager
Canada, Clinical Research Project Manager
Canada, Expanding European Pharmaceuticals firm seeks exeptional Clinical Project Manager for lead role.
Canada, Global Brand Lead for an actively growing Business Unit
Canada, Global Brand Lead for an actively growing Business Unit
Croatia Back to Top
Croatia, Regulatory affairs Specialist - Croatia/Serbia
Europe Back to Top
Europe, Global Head Pharmacovigilance - Europe
Europe, Senior European Quality Program Manager
Europe, Senior European Quality Program Manager
Europe, Specialist Regulatory affairs - Medical Device - Europe
France Back to Top
France, Freelance/ Contract Clinical Research Associate – 12 months+ - 1.0FTE – Paris
France, GCP Consultant – 8 month – 1.0FTE – Office-based, Paris
France, Pharmacovigilance Manager/Specialist - Paris - Biotech
France, Regulatory Affairs Manager - BioTech - Paris
Germany Back to Top
Germany, Freelance Clinical Data Manager – 6 months – Munich, Germany
Germany, Freelance Clinical Trial Manager – 12 Months - Germany
Germany, Freelance Safety Specialist – 1.0FTE – 10 Months Contract – Dusseldorf, Germany.
Germany, Freelance Sales Training Manager – 6 months – 0.8FTE – Germany
Germany, Lead Study Monitor – 1.0FTE - 12 Months – Berlin, Germany
Germany, MSL - Gynaecology and Women's Health - Germany
Germany, MSL in Oncology - Germany
Germany, Qualified Person – 12 months contract – Various Locations (UK, Germany)
Germany, Qualified Person (QP) – 12 Months – Germany
Germany, Qualified Person (QP) – 6 Month Contract – Hamburg, Germany
Switzerland Back to Top
Switzerland, Cleaning and Validation Process Engineer consultant – 1.0FTE – 6 months – Switzerland
Switzerland, Freelance Clinical Trial Coordinator – 1.0FTE – 12 months – Nyon, Switzerland
Switzerland, Freelance Medical Advisor – 0.6FTE – 6 Month Contract - Switzerland
Switzerland, Freelance Qualified Person – 6 Months - 1.0FTE - Switzerland
Switzerland, Freelance Quality Assurance Manager - 6 month - Switzerland
Switzerland, Product Manager - Switzerland - Geneva/Zurich
Switzerland, Quality Assurance Assistant – Switzerland
Switzerland, Verification and Validation Expert Consultant – 6 month – Switzerland – Medical Device
US- Back to Top
US-, Associate Director of Quality Assurance (GMP)
US-, Associate Director, Regulatory Affairs - Advertising and Promotion
US-, Associate Director, Regulatory Affairs - Advertising and Promotion
US-, Associate Director/Quality Engineer for top Pharmaco!
US-, Brand Manager-Benelux
US-, CMC Manager
US-, CMC Regulatory Director
US-, Chief Medical Officer - Basel
US-, Cleaning and Validation Process Engineer consultant – 1.0FTE – 6 months – Switzerland
US-, Clinical Research Associate (CRA) - 1.0 FTE – United Kingdom.
US-, Clinical Research Associate
US-, Contract Clinical Research Associate - Device
US-, Contract Quality Assurance (QA) Manager – 12 months – United Kingdom
US-, Country Manager DACH Region
US-, Director of Quality Assurance (GMP)
US-, Drug Safety Officer
US-, Exceptional CRA for leadership position covering sites across the East Coast
US-, Freelance Clinical Data Manager – 6 months – Munich, Germany
US-, Freelance Clinical Research Physician – United Kingdom – 1.0FTE
US-, Freelance Clinical Study Consultant – 12 months – 1.0FTE – Frankfurt
US-, Freelance Clinical Trial Assistant – 6 months – Cambridge, United Kingdom
US-, Freelance Clinical Trial Coordinator – 1.0FTE – 12 months – Nyon, Switzerland
US-, Freelance Clinical Trial Manager – 12 Months - Germany
US-, Freelance Medical Advisor – 0.6FTE – 6 Month Contract - Switzerland
US-, Freelance Qualified Person – 6 Months - 1.0FTE - Switzerland
US-, Freelance Quality Assurance Consultant - Ukraine - Homebased
US-, Freelance Quality Assurance Consultant in Medical Devices
US-, Freelance Quality Assurance Manager - 6 month - Switzerland
US-, Freelance Safety Specialist – 1.0FTE – 10 Months Contract – Dusseldorf, Germany.
US-, Freelance Sales Training Manager – 6 months – 0.8FTE – Germany
US-, Freelance Senior CRA for Global leading CRO -Homebased- 6 month contract - 1 FTE
US-, Freelance Senior Regulatory Affairs CMC Manager – 1.0FTE - 12 month – Maidenhead
US-, Freelance/ Contract Clinical Research Associate – 12 months+ - 1.0FTE – Paris
US-, Freelance/ Contract Safety Risk Management Manager – 1.0FTE – 12 months – Munich
US-, Freelance/Contract Clinical Safety Manager – 1.0FTE – 12 months – Munich
US-, GCP Consultant – 8 month – 1.0FTE – Office-based, Paris
US-, Global Head Pharmacovigilance - Europe
US-, Growing European Pharmaceuticals firm seeks exceptional Clinical Research Associate
US-, Head Case Processing
US-, Head of Key Account Management
US-, Home-based CRA - CNS
US-, Interim Qualified Person - Belgium
US-, Junior Regulatory Affairs
US-, Key Account Managers
US-, Lead Study Monitor – 1.0FTE - 12 Months – Berlin, Germany
US-, Lead Technical Architect
US-, MSL - Gynaecology and Women's Health - Germany
US-, MSL in Oncology - Germany
US-, Medical Manager
US-, Network Security Specialist
US-, Operational Risk Officer
US-, Partner Manager
US-, Pharmacovigilance Manager/Specialist - Paris - Biotech
US-, Preclinical Drug Development Consultants
US-, Product Manager - Switzerland - Geneva/Zurich
US-, QA Manager – CMO’s / GMP
US-, QA Specialist - Austria
US-, Qualified Person – 12 months contract – Various Locations (UK, Germany)
US-, Qualified Person (QP) – 12 Months – Germany
US-, Qualified Person (QP) – 12 Months - United Kingdom
US-, Qualified Person (QP) – 6 Month Contract – Hamburg, Germany
US-, Quality Assurance (QA) Consultant– Full time – 12 months – London, United Kingdom.
US-, Quality Assurance Assistant – Switzerland
US-, Quality Assurance Manager - Medical Device - Austria
US-, Quality Assurance Manager Opportunity - Belgium - Leading global pharma company
US-, Quality Assurance Specialist - Basel - (CHF) 90,000
US-, Quality Validation and Verification specialist
US-, Quality Validation and Verification specialist
US-, Regional Quality Manager
US-, Regional Sr. Clinical Research Associate
US-, Regulatory Affairs - Associate Director
US-, Regulatory Affairs Manager - BioTech - Paris
US-, Regulatory Director (FDA/EPA) New Projects-Pharma
US-, Regulatory affairs Specialist - Croatia/Serbia
US-, Senior CRA
US-, Senior Drug Safety Consultant – United Kingdom – 12 Months
US-, Senior European Quality Program Manager
US-, Senior European Quality Program Manager
US-, Senior Key Account Manager
US-, Senior MSL - Belgium
US-, Senior MSL - Belgium
US-, Senior Product Manager
US-, Senior Project Manager Pharmaceutical Strategy
US-, Senior Regulatory affairs specialist
US-, Specialist Regulatory affairs - Medical Device - Europe
US-, Verification and Validation Expert Consultant – 6 month – Switzerland – Medical Device
US-, voLTE Specialist
US-AZ Back to Top
US-AZ, Contract Clinical Trial Manager
US-AZ, Contract Clinical Trial Manager
US-AZ, Contract Clinical Trial Manager
US-AZ, Contract Clinical Trial Manager
US-AZ, Director/Executive Director of Clinical Development
US-CA Back to Top
US-CA, VP Pharmacovigilance / Head of Safety
US-CA, Consultant Senior QA Specialist / QA Manager - Menlo Park - Biotech
US-CA, Consultant Senior QA Specialist / QA Manager - Menlo Park - Biotech
US-CA, 18-Month Device Sr. CRA
US-CA, 18-Month Device Sr. CRA
US-CA, Associate Director/Quality Engineer for top Pharmaco!
US-CA, Associate Director/Quality Engineer for top Pharmaco!
US-CA, Asst. Director Quality Management
US-CA, Asst. Director Quality Management
US-CA, CRA II/Sr. CRA
US-CA, Clinical Consultant – Biotech – Sponsor – San Francisco
US-CA, Clinical Consultant – Biotech – Sponsor – San Francisco
US-CA, Clinical Data Manager
US-CA, Clinical Data Manager
US-CA, Clinical Data Manager
US-CA, Clinical Data Manager
US-CA, Clinical Data Manager
US-CA, Clinical Data Manager
US-CA, Clinical Laboratory Scientist - Irvine, CA
US-CA, Clinical Program Manager
US-CA, Clinical Program Manager
US-CA, Clinical Project Manager(Clinical Trials Manager)
US-CA, Clinical Project Manager
US-CA, Clinical Research Associate – Oncology – Phase II and Phase III Trials
US-CA, Clinical Research Associate – Oncology – Phase II and Phase III Trials
US-CA, Clinical Research Associate – Oncology – Phase II and Phase III Trials
US-CA, Clinical Research Associate – Oncology – Phase II and Phase III Trials
US-CA, Clinical Research Associate – Oncology – Phase II and Phase III Trials
US-CA, Clinical Research Associate – Oncology – Phase II and Phase III Trials
US-CA, Clinical Research Associate
US-CA, Clinical Research Medical Director- Bone and Nephrology for a Top Global Pharmaceutical Company
US-CA, Clinical Research Medical Director- Bone and Nephrology for a Top Global Pharmaceutical Company
US-CA, Clinical Site Manager – South San Francisco – Contract – Biotech – 12 month+
US-CA, Clinical Site Manager – South San Francisco – Contract – Biotech – 12 month+
US-CA, Clinical Trial Manager
US-CA, Clinical Trial Manager
US-CA, Clinical Trial Manager
US-CA, Clinical Trial Manager
US-CA, Clinical Trial Manager
US-CA, Clinical Trial Manager
US-CA, Consultant Senior QA Specialist / QA Manager - Menlo Park - Biotech
US-CA, Consultant Senior QA Specialist / QA Manager - Menlo Park - Biotech
US-CA, Contract - QA GLP Auditor – California – 12 months – 0.5 FTE
US-CA, Contract - QA GLP Auditor – California – 12 months – 0.5 FTE
US-CA, Contract CRA – Medical Device – 0.5 FTE – CRO - California
US-CA, Contract CRA – Medical Device – 0.5 FTE – CRO - California
US-CA, Contract CRA – Orange County – Temp to Perm – Medical Device
US-CA, Contract CRA – Orange County – Temp to Perm – Medical Device
US-CA, Contract CTA – Sponsor – San Francisco – 6 month contract
US-CA, Contract CTA – Sponsor – San Francisco – 6 month contract
US-CA, Contract CTA
US-CA, Contract CTA
US-CA, Contract Clinical Research Associate I (CRA I)
US-CA, Contract Clinical Research Associate I (CRA I)
US-CA, Contract Clinical Research Associate II (CRA II)
US-CA, Contract Clinical Research Associate II (CRA II)
US-CA, Contract Clinical Trial Manager
US-CA, Contract Clinical Trial Manager
US-CA, Contract Clinical Trial Manager
US-CA, Contract Clinical Trial Manager
US-CA, Contract Clinical Trial Manager
US-CA, Contract Clinical Trial Manager
US-CA, Contract Clinical Trial Manager
US-CA, Contract Clinical Trial Manager
US-CA, Contract Device CRA
US-CA, Contract Document Formatter, Regulatory Operations
US-CA, Contract Document Formatter, Regulatory Operations
US-CA, Contract Lead Clinical Research Associate
US-CA, Contract Lead Clinical Research Associate
US-CA, Contract Senior CRA – Menlo Park – 6 month contract – Medical Device
US-CA, Contract Senior CRA – Menlo Park – 6 month contract – Medical Device
US-CA, Contract Senior CRA
US-CA, Contract Senior CRA
US-CA, Contract Senior Clinical Research Associate (Sr. CRA)
US-CA, Contract Senior Clinical Research Associate (Sr. CRA)
US-CA, Contract Senior Clinical Research Associate
US-CA, Contract Senior Clinical Research Associate
US-CA, Contract Senior Clinical Trial Manager
US-CA, Contract Senior Clinical Trial Manager
US-CA, Contract Sr. Clinical Trial Manager
US-CA, Contract Sr. Clinical Trial Manager
US-CA, Director Clinical Development - Oncology / Hematology
US-CA, Director Regulatory Affairs
US-CA, Director Regulatory Affairs
US-CA, Director of Regulatory Affairs
US-CA, Director, Program Management for a growing Pharmaceutical Company
US-CA, Director, Program Management for a growing Pharmaceutical Company
US-CA, Drug Safety Associate
US-CA, Freelance/Contract Clinical Trial Manager – Bay Area – 6 month contract with extensions
US-CA, Freelance/Contract Clinical Trial Manager – Bay Area – 6 month contract with extensions
US-CA, Global Regulatory Affairs Executive Director Oncology
US-CA, Global Regulatory Affairs Executive Director Oncology
US-CA, Head of Safety Operations
US-CA, Head of Safety Science
US-CA, Medical Director - Clinical Development - Oncology / Hematology
US-CA, Medical Director - Pharmacovigilance / Drug Safety
US-CA, Medical Director- Clinical Development -Oncology
US-CA, Project Manager/Sr. Project Manager
US-CA, Project Manager/Sr. Project Manager
US-CA, Regulatory Affairs - Associate Director
US-CA, Regulatory Affairs - Associate Director
US-CA, Regulatory Specialist
US-CA, SCRA and CRA II Opportunities - Device
US-CA, SCRA and CRA II Opportunities - Device
US-CA, Senior Clinical Manager
US-CA, Senior Manager of Clinical Research
US-CA, Senior Manager/Associate Director QA needed for VC-backed Biotech Firm
US-CA, Senior Manager/Associate Director QA needed for VC-backed Biotech Firm
US-CA, Senior Regulatory Affairs Specialist
US-CA, Senior Regulatory Specialist
US-CA, Senior Regulatory Specialist
US-CA, Senior Statistical Programmer
US-CA, Senior Statistical Programmer
US-CA, Sr. Clinical Trial Manager - San Francisco, CA
US-CA, Sr. Clinical Trial Manager - San Francisco, CA
US-CA, Sr. Regulatory Affairs Specialist
US-CA, Sr. Regulatory Affairs Specialist
US-CA, Statistical Programmer
US-CA, Statistical Programmer
US-CA, Sterility Assurance Specialist – Switzerland – until December 2015 – Freelance/Contract
US-CA, Sterility Assurance Specialist – Switzerland – until December 2015 – Freelance/Contract
US-CA, Technical Writer
US-CA, Technical Writer
US-CA, Top Pharmaceuticals firm seeks exceptional Regulatory Affairs Associate Director
US-CO Back to Top
US-CO, Clinical Project manager for boutique CRO
US-CO, Clinical Project manager for boutique CRO
US-CO, Contract Clinical Project Manager
US-CO, Contract Clinical Project Manager
US-CO, Senior Scientist, Pharmacometrics
US-CO, Senior Scientist, Pharmacometrics
US-CT Back to Top
US-CT, Clinical Research Associate – Oncology – Phase II and Phase III Trials
US-CT, Clinical Research Associate – Oncology – Phase II and Phase III Trials
US-CT, Quality Control Manager
US-CT, Quality Control Manager
US-DC Back to Top
US-DC, Clinical Program Manager - Contract
US-DC, Clinical Program Manager - Contract
US-DC, Sr. Vaccine/Biologic Regulatory and Quality Affairs Subject Matter Expert
US-DC, Sr. Vaccine/Biologic Regulatory and Quality Affairs Subject Matter Expert
US-DE Back to Top
US-DE, Sr. CRA, Oncology
US-DE, Sr. CRA, Oncology
US-Eastern Back to Top
US-Eastern, Corporate Communications & Marketing Specialist – Geneva
US-Eastern, Freelance CRA - Oncology - 0.6FTE
US-Eastern, Freelance CRA - Oncology - 0.6FTE
US-Eastern, LIMS application developer/application analyst required for a rapidly expanding pharma firm
US-Eastern, LIMS application developer/application analyst required for a rapidly expanding pharma firm
US-Eastern, Senior Expert Clinical PK/PD
US-Eastern, Senior Expert Clinical PK/PD
US-Eastern, Senior Sales – Boutique Specialist Niche Solutions Provider – London
US-FL Back to Top
US-FL, Clinical Research Associate – Oncology – Phase II and Phase III Trials
US-FL, Clinical Research Associate – Oncology – Phase II and Phase III Trials
US-FL, Director of Quality Assurance required for rapidly expanding CRO
US-FL, Director of Quality Assurance required for rapidly expanding CRO
US-FL, Quality Assurance Vice President (Global/Latin America)
US-FL, Quality Assurance Vice President (Global/Latin America)
US-IL Back to Top
US-IL, Associate Director, Biostatistics| Pharmaceuticals
US-IL, Associate Director, Biostatistics| Pharmaceuticals
US-IL, Associate Director/Director of Project Management (Quality Assurance)
US-IL, Associate Director/Director of Project Management (Quality Assurance)
US-IL, Associate Director/Director of Quality Assurance (Combination Product)
US-IL, Associate Director/Director of Quality Assurance (Combination Product)
US-IL, Associate Director/Director of Quality Systems (QRM)
US-IL, Associate Director/Director of Quality Systems (QRM)
US-IL, C++ Software Developer/Engineer – Medical Device
US-IL, C++ Software Developer/Engineer – Medical Device
US-IL, Clinical Research Associate – Oncology – Phase II and Phase III Trials
US-IL, Clinical Research Associate – Oncology – Phase II and Phase III Trials
US-IL, Director/Senior Director of Global Surveillance and Epidemiology (Pharmacovigilance)
US-IL, Director/Senior Director of Global Surveillance and Epidemiology (Pharmacovigilance)
US-IL, Electrical Engineer/Software Developer needed for top Global Pharmaceutical Company!
US-IL, Electrical Engineer/Software Developer needed for top Global Pharmaceutical Company!
US-IL, Global Medical Affairs Director-Oncology
US-IL, Global Medical Affairs Director-Oncology
US-IL, Global Regulatory Affairs Executive Director Oncology
US-IL, Global Regulatory Affairs Executive Director Oncology
US-IL, Global Regulatory Affairs Executive Director Oncology
US-IL, Global Regulatory Affairs Executive Director Oncology
US-IL, Global Regulatory Affairs Executive Director Oncology
US-IL, Global Regulatory Affairs Executive Director Oncology
US-IL, Global Regulatory Affairs Executive Director Oncology
US-IL, Global Regulatory Affairs Executive Director Oncology
US-IL, Group Medical Director | Oncology Clinical Development
US-IL, Group Medical Director | Oncology Clinical Development
US-IL, Health Economics & Outcomes Research Director
US-IL, Health Economics & Outcomes Research Director
US-IL, Internal Auditor, Global Pharmaceutical Leader
US-IL, Lead Research Statistician
US-IL, Leading global Biopharmaceutical firm seeks Two Medical Science Liaison's to manage Midwest territory
US-IL, Leading global Biopharmaceutical firm seeks Two Medical Science Liaison's to manage Midwest territory
US-IL, Medical Science Liaison (MSL)
US-IL, Medical Science Liaison
US-IL, Medical Science Liaison
US-IL, Medical Science Liaison
US-IL, Medical Science Liaison
US-IL, Principal Quality Engineer needed for top Global Pharmaceutical Company!
US-IL, Principal Quality Engineer needed for top Global Pharmaceutical Company!
US-IL, Regulatory Affairs - Director for leading Pharmaceutical firm
US-IL, Regulatory Affairs - Director for leading Pharmaceutical firm
US-IL, Regulatory Affairs Director for leading Pharmaceutical firm
US-IL, Regulatory Affairs Director for leading Pharmaceutical firm
US-IL, Regulatory Affairs Director-Oncology
US-IL, Regulatory Affairs Director-Oncology
US-IL, Regulatory Affairs Manager, CMC - Medical Device
US-IL, Regulatory Affairs Manager, CMC - Medical Device
US-IL, SAS Programmer Assistant Director
US-IL, Senior Medical Director-Neurosciences,Oncology,Immunology, Regulatory Affairs
US-IL, Senior Medical Director-Neurosciences,Oncology,Immunology, Regulatory Affairs
US-IL, Senior Quality Engineer needed for Top Tier Pharmaceutical Company!
US-IL, Senior Quality Engineer needed for Top Tier Pharmaceutical Company!
US-IN Back to Top
US-IN, Clinical Research Associate – Oncology – Phase II and Phase III Trials
US-IN, Clinical Research Associate – Oncology – Phase II and Phase III Trials
US-IN, Medical Science Liaison
US-IN, Medical Science Liaison
US-KY Back to Top
US-KY, Principal Fire Engineer - London, UK
US-LA Back to Top
US-LA, Medical Director-Psychiatry
US-LA, Medical Director-Psychiatry
US-MA Back to Top
US-MA, Associate Director-Publications
US-MA, Associate Director-Publications
US-MA, Biostatistician, Contract
US-MA, Biostatistician, Contract
US-MA, Clinical Project Manager| Oncology
US-MA, Clinical Project Manager| Oncology
US-MA, Clinical Research Associate – Oncology – Phase II and Phase III Trials
US-MA, Clinical Research Associate – Oncology – Phase II and Phase III Trials
US-MA, Clinical Study Manager
US-MA, Clinical Study Manager
US-MA, Contract Biostatistician - Leading Biopharmaceutical Company
US-MA, Contract Biostatistician - Leading Biopharmaceutical Company
US-MA, Contract CRA - remote, oncology
US-MA, Contract CRA - remote, oncology
US-MA, Deviation Investigation Writer for a fastest Growing Contract Manufacturer on the East Coast!
US-MA, Deviation Investigation Writer for a fastest Growing Contract Manufacturer on the East Coast!
US-MA, Director Pharmacometrics/Clinical PK/PD
US-MA, Director Pharmacometrics/Clinical PK/PD
US-MA, Director of Quality Assurance
US-MA, Director of Quality Assurance
US-MA, Engineer Lead/Director of Process Engineering
US-MA, Engineer Lead/Director of Process Engineering
US-MA, Excellent Medical Director needed for top tier firm!
US-MA, Executive Director of R&D Quality Assurance
US-MA, Executive Director of R&D Quality Assurance
US-MA, Global Regulatory Affairs Executive Director Oncology
US-MA, Global Regulatory Affairs Executive Director Oncology
US-MA, Global Regulatory Affairs Executive Director Oncology
US-MA, Global Regulatory Affairs Executive Director Oncology
US-MA, Global Regulatory Affairs Executive Director Oncology
US-MA, Global Regulatory Affairs Executive Director Oncology
US-MA, Global Regulatory Affairs Executive Director
US-MA, Global Regulatory Affairs Executive Director
US-MA, Global Regulatory Lead (Director-Level)
US-MA, Global Regulatory Lead (Director-Level)
US-MA, Global Regulatory Lead (Director-Level)
US-MA, Global Regulatory Lead (Director-Level)
US-MA, IVD Clinical Operations Manager
US-MA, IVD Clinical Operations Manager
US-MA, Medical Director - Oncology
US-MA, Medical Director - Oncology
US-MA, Medical Reviewer, Drug Safety, Needed for top tier Biotech!
US-MA, Medical Reviewer, Drug Safety, Needed for top tier Biotech!
US-MA, QC Supervisor with Raw Materials experience needed for top tier firm!
US-MA, Regulatory Affairs Manager
US-MA, Regulatory Affairs Manager
US-MA, Senior Director of Global Market Access - Global Oncology
US-MA, Senior Director of Global Market Access - Global Oncology
US-MA, Senior Manager/Associate Director of Manufacturing
US-MA, Senior Manager/Associate Director of Manufacturing
US-MA, Senior Principal SAS programmer needed for multi-billion dollar organization
US-MA, Senior Principal SAS programmer needed for multi-billion dollar organization
US-MA, Sr. CRA for ophthalmic studies in Boston
US-MA, Sr. CRA for ophthalmic studies in Boston
US-MA, Sr. Clinical Trial Manager
US-MA, Sr. Clinical Trial Manager
US-MA, Sr. Medical Director-Medical Affairs (Life Cycle Management)
US-MA, Sr. Medical Director-Medical Affairs (Life Cycle Management)
US-MD Back to Top
US-MD, Quantitative Data Manager | Investment Management
US-MD, Senior Project Manager –Data Gov. & Architecture
US-MD, Sr. Drug Safety Specialist | Pharmacovigilance (PV)
US-MD, Sr. Drug Safety Specialist | Pharmacovigilance (PV)
US-MO Back to Top
US-MO, Formulations Scientist
US-MO, Formulations Scientist
US-MO, Web Content Manager
US-NC Back to Top
US-NC, CMC Regulatory Director
US-NC, CMC Regulatory Director
US-NC, Clinical Research Associate – Oncology – Phase II and Phase III Trials
US-NC, Clinical Research Associate – Oncology – Phase II and Phase III Trials
US-NC, Clinical Research Associate – Oncology – Phase II and Phase III Trials
US-NC, Clinical Research Associate – Oncology – Phase II and Phase III Trials
US-NC, Clinical Research Associate
US-NC, Clinical Research Associate
US-NC, Director, Regulatory Affairs CMC
US-NC, Director, Regulatory Affairs CMC
US-NH Back to Top
US-NH, Quality Control Scientist Raw Materials
US-NH, Quality Control Scientist Raw Materials
US-NJ Back to Top
US-NJ, Associate Director Regulatory Affairs
US-NJ, Associate Director Regulatory Affairs
US-NJ, Associate Director of Biostatistics for a rapidly growing independent CRO
US-NJ, Associate Director of Biostatistics for a rapidly growing independent CRO
US-NJ, Associate Director of Clinical and Medical Quality needed for Top Five Global Pharmaceutical Company!
US-NJ, Associate Director of Clinical and Medical Quality needed for Top Five Global Pharmaceutical Company!
US-NJ, Associate Director of Sales Operations – Global Pharmaceutical Company
US-NJ, Associate Director of Sales Operations – Global Pharmaceutical Company
US-NJ, Clinical Project Manager| Oncology
US-NJ, Clinical Project Manager| Oncology
US-NJ, Clinical Research Associate – Oncology – Phase II and Phase III Trials
US-NJ, Clinical Research Associate – Oncology – Phase II and Phase III Trials
US-NJ, Clinical Research Associate at international Pharma company
US-NJ, Clinical Research Associate at international Pharma company
US-NJ, Director of Clinical and Medical Quality needed for Top Five Global Pharmaceutical Company!
US-NJ, Director of Clinical and Medical Quality needed for Top Five Global Pharmaceutical Company!
US-NJ, Director of Immunology Marketing – One hundred billion dollar pharmaceuticals firm
US-NJ, Director of Immunology Marketing – One hundred billion dollar pharmaceuticals firm
US-NJ, Director of Retail Marketing – One hundred billion dollar pharmaceuticals firm
US-NJ, Director of Retail Marketing – One hundred billion dollar pharmaceuticals firm
US-NJ, Director of Sales & Marketing Analytics – Global Pharma Brand
US-NJ, Director of Sales & Marketing Analytics – Global Pharma Brand
US-NJ, Global Head of Regulatory Affairs
US-NJ, Global Head of Regulatory Affairs
US-NJ, Global Medical Director - Endocrinology – New Jersey
US-NJ, Global Medical Director - Endocrinology – New Jersey
US-NJ, Global Medical Director Endocrinology – New Jersey
US-NJ, Global Medical Director Endocrinology – New Jersey
US-NJ, Global Medical Director for a Top Global Pharmaceutical Company
US-NJ, Global Medical Director for a Top Global Pharmaceutical Company
US-NJ, Global Program Medical Director - CVM
US-NJ, Global Program Medical Director
US-NJ, Global Regulatory Strategist
US-NJ, Global Regulatory Strategist
US-NJ, Junior to Senior Clinical Biostatisticians| SAS Programmers Needed
US-NJ, Junior to Senior Clinical Biostatisticians| SAS Programmers Needed
US-NJ, Lead CRA
US-NJ, Lead CRA
US-NJ, Multiple Field Communications Specialist Roles Available
US-NJ, Multiple Field Communications Specialist Roles Available
US-NJ, Principal Biostatistician Manager needed for one of the worlds most innovative firms
US-NJ, Principal Biostatistician for a rapidly growing independent CRO
US-NJ, Principal Biostatistician for a rapidly growing independent CRO
US-NJ, Principal Statistical SAS Programmer Analyst for a rapidly expanding CRO
US-NJ, Principal Statistical SAS Programmer Analyst for a rapidly expanding CRO
US-NJ, R&D Program Manager
US-NJ, R&D Program Manager
US-NJ, Senior Biostatistician for a Rapidly Growing Independent CRO
US-NJ, Senior Biostatistician for a Rapidly Growing Independent CRO
US-NJ, Senior Development Scientist for top 5 pharma firm
US-NJ, Senior Development Scientist for top 5 pharma firm
US-NJ, Senior Global Clinical Program Manager
US-NJ, Senior Global Clinical Program Manager
US-NJ, Senior Manager of Biostatistics
US-NJ, Senior Manager/Associate Director of Manufacturing
US-NJ, Senior Manager/Associate Director of Manufacturing
US-NJ, Senior Statistical Programmer for a rapidly expanding CRO
US-NJ, Senior Statistical Programmer for a rapidly expanding CRO
US-NJ, Site Quality Head for a fastest Growing Pharmaceutical Company!
US-NJ, Site Quality Head for a fastest Growing Pharmaceutical Company!
US-NJ, Sr. Clinical Trial Manager - Princeton, NJ
US-NJ, Sr. Clinical Trial Manager - Princeton, NJ
US-NJ, Sr. Manager Regulatory Affairs - Medical Device
US-NJ, Sr. Manager Regulatory Affairs - Medical Device
US-NJ, Sr. Principal Biostatistician
US-NJ, Sr. Product Manager - Process Commercialization
US-NJ, Sr. Product Manager - Process Commercialization
US-NJ, Sr. Scientist III (PhD)
US-NJ, Sr. Scientist III (PhD)
US-NJ, Statistical Programmer Contractor
US-NJ, Statistical Programmer Contractor
US-NJ, Statistical Programmer for a rapidly expanding CRO
US-NJ, Statistical Programmer for a rapidly expanding CRO
US-NJ, Statistical Programming Manager
US-NV Back to Top
US-NV, Freelance Quality Assurance Manager
US-NV, Freelance Quality Assurance Manager
US-NY Back to Top
US-NY, Assistant Director - Quality GCP
US-NY, Business Development – Life Sciences Recruitment
US-NY, Chief Medical Officer
US-NY, Chief Medical Officer
US-NY, Clinical Research Associate – Oncology – Phase II and Phase III Trials
US-NY, Clinical Research Associate – Oncology – Phase II and Phase III Trials
US-NY, Clinical Trial Assistant/Clinical Project Associate
US-NY, Clinical Trial Assistant/Clinical Project Associate
US-NY, Clinical Trial Support Coordinator
US-NY, Clinical Trial Support Coordinator
US-NY, Contract Regional Sr. Clinical Research Associate
US-NY, Contract Regional Sr. Clinical Research Associate
US-NY, Director of Generic Drug Marketing
US-NY, Director of Generic Drug Marketing
US-NY, Director of Generic Drug Marketing
US-NY, Director of Generic Drug Marketing
US-NY, Director of Sales & Marketing Analytics – Leading Pharmaceutical Company
US-NY, Director of Sales & Marketing Analytics – Leading Pharmaceutical Company
US-NY, Executive Director Regulatory Affairs
US-NY, Executive Director Regulatory Affairs
US-NY, Front End Developer
US-NY, Global Regulatory Affairs Executive Director Oncology
US-NY, Global Regulatory Affairs Executive Director Oncology
US-NY, Home-Based CRA - 4-year Contract
US-NY, Home-Based CRA - 4-year Contract
US-NY, Java Developer, Risk & Pricing - Investment Bank
US-NY, LIMS Research - Technical Lead Manager
US-NY, LIMS Research - Technical Lead Manager
US-NY, Medical Affairs Director Biosimilars
US-NY, Medical Affairs Director Biosimilars
US-NY, Medical Affairs Director Biosimilars
US-NY, Medical Affairs Director Biosimilars
US-NY, Multiple Roles In Pharmacovigilance
US-NY, Multiple Roles In Pharmacovigilance
US-NY, Predictive Analytics Developer –Real-time Equities
US-NY, Project lead Clinical PK/PD
US-NY, Project lead Clinical PK/PD
US-NY, Senior Director of Quality Assurance (GCP) needed for top Pharmaceutical Company!
US-NY, Senior Director of Quality Assurance (GCP) needed for top Pharmaceutical Company!
US-NY, Vice President – Tunnelling. USA (Any Location)
US-NY, iOS Developer
US-Nationwide Back to Top
US-Nationwide, Associate Director of Quality Assurance (GMP)
US-Nationwide, Associate Director, Regulatory Affairs - Advertising and Promotion
US-Nationwide, Associate Director, Regulatory Affairs - Advertising and Promotion
US-Nationwide, Associate Director/Quality Engineer for top Pharmaco!
US-Nationwide, Brand Manager-Benelux
US-Nationwide, CMC Manager
US-Nationwide, CMC Regulatory Director
US-Nationwide, Chief Medical Officer - Basel
US-Nationwide, Clinical Research Associate (CRA) - 1.0 FTE – United Kingdom.
US-Nationwide, Clinical Research Associate
US-Nationwide, Contract Quality Assurance (QA) Manager – 12 months – United Kingdom
US-Nationwide, Country Manager DACH Region
US-Nationwide, Director of Quality Assurance (GMP)
US-Nationwide, Drug Safety Officer
US-Nationwide, Freelance Clinical Research Physician – United Kingdom – 1.0FTE
US-Nationwide, Freelance Clinical Study Consultant – 12 months – 1.0FTE – Frankfurt
US-Nationwide, Freelance Clinical Trial Assistant – 6 months – Cambridge, United Kingdom
US-Nationwide, Freelance Quality Assurance Consultant - Ukraine - Homebased
US-Nationwide, Freelance Quality Assurance Consultant in Medical Devices
US-Nationwide, Freelance Senior CRA for Global leading CRO -Homebased- 6 month contract - 1 FTE
US-Nationwide, Freelance Senior Regulatory Affairs CMC Manager – 1.0FTE - 12 month – Maidenhead
US-Nationwide, Freelance/ Contract Safety Risk Management Manager – 1.0FTE – 12 months – Munich
US-Nationwide, Freelance/Contract Clinical Safety Manager – 1.0FTE – 12 months – Munich
US-Nationwide, Head Case Processing
US-Nationwide, Home-based CRA - CNS
US-Nationwide, Junior Regulatory Affairs
US-Nationwide, Medical Manager
US-Nationwide, Preclinical Drug Development Consultants
US-Nationwide, QA Manager – CMO’s / GMP
US-Nationwide, Qualified Person (QP) – 12 Months - United Kingdom
US-Nationwide, Quality Assurance (QA) Consultant– Full time – 12 months – London, United Kingdom.
US-Nationwide, Quality Assurance Specialist - Basel - (CHF) 90,000
US-Nationwide, Quality Validation and Verification specialist
US-Nationwide, Quality Validation and Verification specialist
US-Nationwide, Regional Quality Manager
US-Nationwide, Regional Sr. Clinical Research Associate
US-Nationwide, Regulatory Director (FDA/EPA) New Projects-Pharma
US-Nationwide, Senior CRA
US-Nationwide, Senior Drug Safety Consultant – United Kingdom – 12 Months
US-Nationwide, Senior Key Account Manager
US-Nationwide, Senior Product Manager
US-Nationwide, Senior Project Manager Pharmaceutical Strategy
US-Nationwide, Senior Regulatory affairs specialist
US-North Back to Top
US-North, Principal Fire Engineer - Bicester, UK
US-OH Back to Top
US-OH, Associate Director-Regulatory Publishing
US-OH, Associate Director-Regulatory Publishing
US-OH, Home-Based CRA - 2 Year Contract
US-OH, Home-Based CRA - 2 Year Contract
US-OH, Leading global Biopharmaceutical firm seeks Two Medical Science Liaison's to manage Midwest territory
US-OH, Leading global Biopharmaceutical firm seeks Two Medical Science Liaison's to manage Midwest territory
US-OH, Medical Science Liaison
US-OH, Medical Science Liaison
US-OH, Multiple Regulatory Affair Manager to Director Available
US-OH, Multiple Regulatory Affair Manager to Director Available
US-OH, Multiple Regulatory Affairs Manager to Director Available
US-OH, Multiple Regulatory Affairs Manager to Director Available
US-OH, Ohio Home-Based CRA
US-OH, Ohio Home-Based CRA
US-OH, Principal Medical Writer
US-OH, Principal Medical Writer
US-OH, Senior Clinical Research Associate-Oncology
US-OH, Senior Clinical Research Associate-Oncology
US-PA Back to Top
US-PA, Clinical Research Associate – Oncology – Phase II and Phase III Trials
US-PA, Clinical Research Associate – Oncology – Phase II and Phase III Trials
US-PA, Data Scientist
US-PA, Data Scientist
US-PA, Principal Biostatistician wanted for innovative firm!
US-PA, Sterilization Consultant - 12 month contract position
US-PA, Sterilization Consultant - 12 month contract position
US-PA, US based Pharmaceutical company with huge growth projection seeks Clinical Data Manager
US-PA, US based Pharmaceutical company with huge growth projection seeks Clinical Data Manager
US-SC Back to Top
US-SC, Clinical Research Associate – Oncology – Phase II and Phase III Trials
US-SC, Clinical Research Associate – Oncology – Phase II and Phase III Trials
US-Southeast Back to Top
US-Southeast, Regional Sales Manager
US-Southeast, Regional Sales Manager
US-TX Back to Top
US-TX, Associate Director/Quality Engineer for top Pharmaco!
US-TX, Associate Director/Quality Engineer for top Pharmaco!
US-WV Back to Top
US-WV, Technical Area Lead / Manager of Manufacturing & Operations
US-WV, Technical Area Lead / Manager of Manufacturing & Operations
US-WV, Technical Area Lead / Supervisor of Manufacturing & Operations
US-WV, Technical Area Lead / Supervisor of Manufacturing & Operations