Regulatory Start-up/Site Activation Specialist

Key QualificationsBachelor's Degree in a Relevant Field2 Years of Clinical Research Experience or Equivalent Combination of Education, Training, and ExperienceThorough Knowledge of Clinical Systems, Procedures, and Corporate StandardsStrong Understanding of Medical Terminology and RegulationsBroad Knowledge of Clinical ResearchProficiency in Microsoft Office...

About the RoleSyneos Health is a leading biopharmaceutical solutions organization that accelerates customer success. As a Site Activation Lead, you will play a critical role in ensuring the successful activation of clinical trial sites, collaborating with cross-functional teams to identify and evaluate site start-up issues, and developing and maintaining...

About the RoleSyneos Health is a leading biopharmaceutical solutions organization that accelerates customer success. As a Site Activation Lead, you will play a critical role in ensuring the successful activation of clinical trial sites, collaborating with cross-functional teams to identify and evaluate site start-up issues, and developing and maintaining...

Key QualificationsWe are seeking a highly skilled Regulatory Start-up/Site Activation Specialist to join our team at IQVIA. The ideal candidate will possess a Bachelor's Degree in a related field and a minimum of 2 years of clinical research experience.Education and Experience: Bachelor's Degree in a related field and 2 years of clinical research experience...

Key QualificationsWe are seeking a highly skilled Regulatory Start-up/Site Activation Specialist to join our team at IQVIA. The ideal candidate will possess a Bachelor's Degree in a related field and a minimum of 2 years of clinical research experience.Education and Experience: Bachelor's Degree in a related field and 2 years of clinical research experience...

About the RoleWe are seeking a highly skilled and experienced Study Start Up Associate to join our team at Sin nombre. As a key member of our Study Start Up Team, you will play a critical role in ensuring that physicians at our research sites are prepared to start clinical trials.Key ResponsibilitiesContract Review and Negotiation: Review and negotiate...

About the RoleWe are seeking a highly skilled and experienced Study Start Up Associate to join our team at Sin nombre. As a key member of our Study Start Up Team, you will play a critical role in ensuring that physicians at our research sites are prepared to start clinical trials.Key ResponsibilitiesContract Review and Negotiation: Review and negotiate...

About the RoleWe are seeking a highly skilled and experienced Study Start Up Associate to join our team at Sin Nombre. As a key member of our Study Start Up Team, you will play a critical role in ensuring that physicians at our research sites are prepared to start clinical trials.Key ResponsibilitiesReview and negotiate clinical site investigator contracts...

About the RoleWe are seeking a highly skilled and experienced Study Start Up Associate to join our team at Sin Nombre. As a key member of our Study Start Up Team, you will play a critical role in ensuring that physicians at our research sites are prepared to start clinical trials.Key ResponsibilitiesReview and negotiate clinical site investigator contracts...

Regulatory Affairs SpecialistALGAKTIV is a biotechnology and microalgae company headquartered in Barcelona, Spain, specializing in skincare products with high-performance active ingredients.We are seeking a highly skilled and motivated Regulatory Affairs Specialist to join our team. This role is crucial in ensuring that our cosmetic products comply with...

Regulatory Affairs SpecialistALGAKTIV is a biotechnology and microalgae company headquartered in Barcelona, Spain, specializing in skincare products with high-performance active ingredients.We are seeking a highly skilled and motivated Regulatory Affairs Specialist to join our team. This role is crucial in ensuring that our cosmetic products comply with...

Company OverviewWorldwide Clinical Trials is a leading global contract research organization (CRO) that partners with biotechnology and pharmaceutical companies to create customized solutions that advance new medications from discovery to reality.Our MissionWe are united in our cause to improve the lives of patients through new and innovative therapies. Our...

Company OverviewWorldwide Clinical Trials is a leading global contract research organization (CRO) that partners with biotechnology and pharmaceutical companies to create customized solutions that advance new medications from discovery to reality.Our MissionWe are united in our cause to improve the lives of patients through new and innovative therapies. Our...

Job Title: Regulatory Affairs SpecialistLocation: Remote (hybrid)Job Description:The Regulatory Affairs Specialist delivers innovative, breakthrough global regulatory strategies for clinical trial registration with health authorities. The RA Specialist is responsible for regulatory aspects related to clinical trial regulatory submissions in alignment with...

Job Title: Regulatory Affairs SpecialistLocation: Remote (hybrid)Job Description:The Regulatory Affairs Specialist delivers innovative, breakthrough global regulatory strategies for clinical trial registration with health authorities. The RA Specialist is responsible for regulatory aspects related to clinical trial regulatory submissions in alignment with...

Job DescriptionJob Title: Regulatory Affairs Specialist - PackagingJob Summary:We are seeking a highly skilled Regulatory Affairs Specialist - Packaging to join our Biopharma Regulatory department at Grifols. As a key member of our team, you will be responsible for ensuring compliance with regulatory standards and guidelines for packaging and labeling of our...

Job DescriptionJob Title: Regulatory Affairs Specialist - PackagingJob Summary:We are seeking a highly skilled Regulatory Affairs Specialist - Packaging to join our Biopharma Regulatory department at Grifols. As a key member of our team, you will be responsible for ensuring compliance with regulatory standards and guidelines for packaging and labeling of our...

Regulatory Affairs SpecialistWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Galderma. As a key member of our Regulatory Affairs department, you will be responsible for preparing and updating CMC dossier sections for assigned products.Key Responsibilities:Contribute to global regulatory CMC strategiesAssess regulatory impact...

Regulatory Affairs SpecialistWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Galderma. As a key member of our Regulatory Affairs department, you will be responsible for preparing and updating CMC dossier sections for assigned products.Key Responsibilities:Contribute to global regulatory CMC strategiesAssess regulatory impact...

Job Title: Regulatory Affairs SpecialistGalderma is a leading dermatology company that is dedicated to advancing the field of dermatology for every skin story. We are seeking a highly skilled Regulatory Affairs Specialist to join our team.Job SummaryThe Regulatory Affairs Specialist will be responsible for delivering innovative, breakthrough global...