Clinical Trial Disclosure Specialist

About the RoleWe are seeking a skilled Clinical Trial Disclosure Specialist to join our team at Lifelancer. The successful candidate will be responsible for coordinating and developing multiple disclosures deliverables, ensuring compliance with industry guidelines and client requirements.Key ResponsibilitiesCoordinate registration, maintenance, and results...

About the RoleLifelancer is seeking a highly skilled Clinical Trials Disclosure Specialist to join our team. As a key member of our team, you will be responsible for coordinating and developing multiple disclosures deliverables, ensuring compliance with industry guidelines and client requirements.Key ResponsibilitiesCoordinate registration, maintenance, and...

Job SummaryThe Clinical Trial Disclosure Specialist will be responsible for coordinating and developing multiple disclosures deliverables, including compliant registry authoring and maintenance of information on public registries, document redaction, and/or plain language authoring, ensuring adherence to relevant industry guidelines and client styles and...

About UsLifelancer is a talent hiring platform in Life Sciences, Pharma, and IT. We connect talent with opportunities in pharma, biotech, health sciences, healthtech, data science, and IT domains.We are seeking a highly skilled Clinical Trial Transparency and Disclosure Specialist to join our team. As a Clinical Trial Transparency and Disclosure Specialist,...

About LifelancerLifelancer is a talent hiring platform in Life Sciences, Pharma, and IT. We connect talent with opportunities in pharma, biotech, health sciences, healthtech, data science, and IT domains.The Clinical Trials Disclosure Specialist position is responsible for the overall coordination and development of multiple disclosures deliverables,...

About the RoleThe Clinical Trial Registration Sr. Specialist will report to the Clinical Trial Registration Lead, responsible for preparing and providing operational support for the registration and maintenance of clinical trials into public registries in US and EU.Key ResponsibilitiesThe successful candidate will drive the processes for assigned protocol...

Job Summary We are seeking a highly skilled Clinical Trial Registration Specialist to join our team at Bristol Myers Squibb. As a key member of our clinical trials operations team, you will be responsible for preparing and providing operational support for the registration and maintenance of clinical trials into public registries in the US and EU. Key...

About This RoleThe Clinical Trial Registration Sr. Specialist will report to the Clinical Trial Registration Lead, providing operational support for the registration and maintenance of clinical trials into public registries in the US and EU.Key ResponsibilitiesDrive the processes for assigned protocol registration activities, ensuring timely and high-quality...

Transforming Patients' Lives through ScienceBristol Myers Squibb is a leading biopharmaceutical company dedicated to transforming patients' lives through science. We are seeking a highly skilled Clinical Trial Registration Specialist to join our team.Job SummaryThe Clinical Trial Registration Specialist will be responsible for preparing and providing...

Transforming Patients' Lives through ScienceBristol Myers Squibb is a leading biopharmaceutical company dedicated to transforming patients' lives through science. We are seeking a highly skilled Clinical Trial Registration Specialist to join our team.Job SummaryThe Clinical Trial Registration Specialist will be responsible for preparing and providing...

Transforming Patients' Lives through ScienceBristol Myers Squibb is a leading pharmaceutical company that is dedicated to transforming patients' lives through science. We are seeking a highly skilled and experienced Senior Specialist Clinical Trial Registration to join our team.Job SummaryThe Senior Specialist Clinical Trial Registration will be responsible...

Job DescriptionThis role is responsible for managing and executing centralized activities in support of global clinical trials, with a focus on clinical documentation. The successful candidate will interact with CROs, vendors, country trial managers, and other stakeholders to ensure compliance with regulatory standards and Bristol Myers Squibb policies.Key...

Job SummaryWe are seeking a skilled Statistical Programmer - Clinical Trials Specialist to join our team at Parexel. As a key member of our statistical programming team, you will be responsible for ensuring the high-quality delivery of statistical programming services for our clients.Key ResponsibilitiesProvide statistical programming support for clinical...

Job DescriptionAs a Clinical Trials Lead at Dr. Reddy's Laboratories Limited, you will be responsible for the preparation and review of critical documents related to clinical trials. Your expertise in clinical pharmacology and regulatory affairs will be crucial in ensuring compliance with regulatory requirements and guidelines.Key ResponsibilitiesPreparation...

Job SummaryAs a Clinical Trials Project Manager at Statistics & Data Corporation (SDC), you will oversee and coordinate all IRT activities in support of clinical and/or non-clinical research studies. This includes managing timelines, budgets, staff, project scope, reports, and communication for the lifecycle of the project(s). You will also mentor and train...

Bristol Myers Squibb is a leading global pharmaceutical company dedicated to discovering, developing, and delivering innovative therapies to patients with serious diseases.Estimated Salary: $120,000 - $180,000 per yearJob DescriptionThis Senior Clinical Trial Management Leader role plays a critical part in our mission by overseeing the execution of clinical...

Transforming Lives through Clinical TrialsBristol Myers Squibb is at the forefront of innovative healthcare solutions, and we're seeking a Senior Manager, Global Submission Management, Clinical Trials to join our team.Key ResponsibilitiesManage a team of direct reports to ensure timely, compliant, and accurate delivery of core submission documents and...

Job Title: Clinical Quality Assurance SpecialistDr. Reddy's Laboratories Limited is seeking a highly skilled Clinical Quality Assurance Specialist to join our team. The successful candidate will be responsible for ensuring the quality and integrity of our clinical trials, as well as developing and implementing quality management systems.Key...

Key ResponsibilitiesAs a Principal Statistical Programmer, you will provide statistical programming support to clinical trials. Your duties will include generating/validating analysis datasets, tables, listings, and figures for clinical trials. You will create SDTM mapping and datasets, develop and maintain the infrastructure for project files of SAS...

Job Title: Principal Statistical ProgrammerJob Summary:Statistics & Data Corporation (SDC) is seeking a highly skilled Principal Statistical Programmer to join our team. As a key member of our biometrics department, you will be responsible for providing statistical programming support to clinical trials. Your expertise will be crucial in producing...