Clinical Operations Specialist with Regulatory Expertise

Job SummaryAs a Senior Clinical Operations Specialist at Syneos Health Clinical, you will play a critical role in ensuring the successful execution of clinical trials. This position requires a strong understanding of clinical trial operations, regulatory compliance, and data management.Key ResponsibilitiesAttend Trusted Process meetings as a subject matter...

{"title": "Clinical Operations Specialist", "content": "**About the Role**Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.**Key Responsibilities**Perform activities...

Job Summary:We are seeking a highly skilled Clinical Trials Due Diligence Specialist to join our team at Syneos Health Clinical. As a key member of our team, you will be responsible for applying your technical expertise to complete and record assigned due diligence tasks.Key Responsibilities:Conduct thorough due diligence reviews of clinical trials and...

{"title": "SSU & Regulatory Specialist with Experience in Clinical Trials", "subtitle": "Join Syneos Health", "content": "**About Us**Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern...

About the RoleWe are seeking a highly skilled Regulatory Specialist to join our team at Syneos - Clinical And Corporate - Prod. As a key member of our team, you will be responsible for ensuring compliance with regulatory requirements and providing high-quality support to our clients.Key ResponsibilitiesProvide quality assurance on deliverables at the country...

Unlock Meaningful Work at Thermo Fisher ScientificAt Thermo Fisher Scientific, you'll discover a career that makes a positive impact on a global scale. Our mission is to enable our customers to make the world healthier, cleaner, and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond...

About Syneos HealthAt Syneos Health, we are a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities.Our Clinical Development model brings the customer and the patient to the center of...

Job OverviewNovasyte is seeking a highly skilled Regulatory Specialist 2 to join our team. As a key member of our clinical research operations team, you will be responsible for performing tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures...

Job SummaryMsd is seeking a highly skilled and experienced Senior Clinical Research Specialist to join our team. As a key member of our clinical research operations, you will be responsible for ensuring the successful execution of clinical trials in assigned countries.Key ResponsibilitiesEnsure compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations,...

Job SummaryWe are seeking a highly skilled Regulatory Affairs Specialist to join our team at Medtronic. As a key member of our regulatory team, you will play a critical role in ensuring the compliance of our medical devices with regulatory requirements in Mexico and Latin America.Key ResponsibilitiesDevelop and implement regulatory strategies to ensure...

About the RoleWe are seeking a highly skilled Regulatory Specialist to join our team at Syneos Health. As a key member of our Clinical Development team, you will be responsible for providing quality deliverables at the country level and ensuring compliance with project requirements and applicable country rules.Key ResponsibilitiesProvide quality on...

**Job Summary**Medpace, Inc. is a leading contract research organization (CRO) providing clinical development services to the biotechnology, pharmaceutical, and medical device industries. We are seeking a highly skilled Clinical Safety Coordinator to join our team in a full-time, office-based position.**Key Responsibilities:**Oversight of submission of...

Job Title: Clinical Research CoordinatorLocation: Houston, TexasCompany: Clinical Trial NetworkPosition Type: Full-timeVisa: TN offeredWe are seeking a highly organized and experienced Clinical Research Coordinator to play a critical role in the planning, implementation, and coordination of clinical research studies conducted within Clinical Trial...

Job SummaryAt ICON, we are seeking a highly skilled Senior Regulatory Affairs Specialist to join our team. As a key member of our regulatory affairs department, you will play a critical role in ensuring compliance with regulatory requirements and facilitating the successful execution of clinical trials.Key ResponsibilitiesLead the preparation, submission,...

About the RoleWe are seeking a highly skilled Clinical Specialist to join our team at Boston Scientific Corporation. As a Clinical Specialist, you will play a critical role in supporting the clinical trials process, ensuring compliance with regulatory and company guidelines, and providing training and education to physicians and hospital staff.Key...

About the RoleWe are seeking a highly skilled and detail-oriented Associate I, TMF Operations Specialist to join our team at Worldwide Clinical Trials. As a key member of our operations team, you will play a critical role in ensuring the quality and integrity of our clinical trial documents.Key ResponsibilitiesProcess Trial Master File (TMF) documents for...

Job Summary:Medpace, a leading clinical contract research organization, is seeking a full-time Clinical Safety Coordinator to support the pharmacovigilance process. This role plays a critical part in ensuring compliance with regulatory timelines and guidelines. The ideal candidate will have a strong understanding of Good Clinical Practice (GCP) guidelines...

Job Summary**Senior Regulatory Affairs Specialist**We are seeking a highly skilled and experienced Senior Regulatory Affairs Specialist to join our team at ICON Plc. As a key member of our regulatory affairs team, you will play a critical role in ensuring the successful execution of clinical trials and contributing to the advancement of innovative treatments...

Job SummaryMsd is seeking a highly skilled and experienced Senior Clinical Research Specialist to join our team. As a key member of our clinical research operations, you will be responsible for ensuring the successful execution of clinical trials in assigned countries.Key ResponsibilitiesEnsure compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations,...

Job SummaryWe are seeking a highly skilled Regulatory Market Operations Oversight Specialist to join our team at Hsbc. As a key member of our operations team, you will be responsible for managing market and regulatory initiatives, ensuring compliance with internal and industry targets.Key ResponsibilitiesManage the delivery of regulatory operational changes...