Clinical Investigator

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 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...

Job SummaryWe are seeking a highly skilled professional to lead the establishment and supervision of quality management systems in clinical development. This role involves strategic planning and execution of audits, ensuring adherence to GxP standards, and driving quality assurance initiatives across diverse systems.Key ResponsibilitiesSupport the...

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 highly skilled Clinical Quality Assurance Associate to join our team at Dr. Reddy's Laboratories Limited. As a Clinical Quality Assurance Associate, you will be responsible for ensuring the quality and compliance of our clinical development processes.Key ResponsibilitiesDevelop and maintain training matrices for clinical...

Job SummaryWe are seeking a highly skilled Clinical Quality Assurance Associate to join our team at Dr. Reddy's Laboratories Limited. As a Clinical Quality Assurance Associate, you will be responsible for developing and maintaining training matrices for each job role in clinical development, ensuring all referenced SOPs and guidance are current and...

Job Title: Associate Director – Bio-Clinical StudiesJob Summary:Ferring Pharmaceuticals is seeking a highly experienced Associate Director to lead clinical and non-clinical projects and provide scientific support on biopharmaceutical development for LBOE & Global projects.Key Responsibilities:Develop and implement clinical and non-clinical study plans to...

Job Title: Scientific Project LeaderJob Summary:We are seeking a highly experienced Scientific Project Leader to lead clinical and non-clinical projects and scientific support on biopharmaceutical development for LBOE & Global projects at Ferring India FHPDC R&D.Key Responsibilities:Plan, conduct, and manage early to late phase clinical development studies...

Job Title: Senior Research Scientist BioClinical Studies ProfessionalJob Summary:Life Sciences talent hiring platform Lifelancer seeks a Senior Research Scientist BioClinical Studies Professional to support projects through proof of concept to clinical development for LBOE Global projects.Key Responsibilities:Develop and manage early to late phase clinical...

Job Title: Senior Global Trial ManagerJob SummaryWe are seeking a Senior Global Trial Manager to join our team at Bristol Myers Squibb. As a Senior Global Trial Manager, you will be responsible for managing clinical trials from initiation to closure, ensuring timely and within-budget delivery of trials.Key ResponsibilitiesLead cross-functional teams to...

About the RoleThe Worldwide Patient Safety group at Bristol Myers Squibb is responsible for ensuring the safety of our medicines. As a Safety Specialist, Regulatory Compliance, you will contribute to pharmacovigilance and pharmaco-epidemiology deliverables, including single case and aggregate safety monitoring, safety reporting, and risk management...

Job Title: Senior Research Associate/Assistant Scientist BioClinical StudiesJob Description:We are seeking a highly skilled Senior Research Associate/Assistant Scientist to join our BioClinical Studies team. The successful candidate will be responsible for supporting and guiding projects through proof of concept to clinical development for LBOE Global...

**Job Title:** Senior Research Associate/Instant Scientist BioClinical Studies**Role:** Support projects from proof of concept to clinical development for LBOE Global projects as a Senior Research Associate/Instant Scientist BioClinical Studies.**Key Responsibilities:**Support synopsis development planning and management of early to late phase clinical...

Job Description:Role: Senior Research Associate/Assistant Scientist Bio Clinical StudiesReporting to: Associate Director BioClinical StudiesLocation: RemoteExperience: At least 7 years of industrial experience in the field of BioClinical Studies with M. Pharma or 4 years of industrial experience with Ph.D.Qualification: M. Pharma/ M.S or Ph.D....

Transforming Lives through Regulatory DocumentationBristol Myers Squibb is at the forefront of transforming the lives of patients worldwide through innovative scientific solutions. As a Senior Scientific Writer I, you will play a pivotal role in contributing to this mission by authoring complex regulatory documents that meet global standards and...

Job Description:Role: Senior Research Associate/Assistant Scientist BioClinical StudiesReporting to: Associate Director BioClinical StudiesLocation: HyderabadExperience: At least 7 years of industrial experience in the field of BioClinical Studies with M.Pharma or 4 years of industrial experience with Ph.D.Qualification: M. Pharma/ M.S or Ph.D....

Job Title: Senior Research Associate/Assistant Scientist BioClinical StudiesJob Summary:We are seeking a highly skilled Senior Research Associate/Assistant Scientist to join our BioClinical Studies team. The successful candidate will be responsible for supporting and guiding projects through proof of concept to clinical development for LBOE Global...

Job Title: Senior Research Associate/Assistant Scientist BioClinical StudiesJob Summary:We are seeking a highly skilled Senior Research Associate/Assistant Scientist to join our BioClinical Studies team. The successful candidate will be responsible for supporting and guiding projects through proof of concept to clinical development for LBOE Global...

Job DescriptionImaging Endpoints is seeking a highly skilled Regulatory Affairs Manager to join our team. As a key member of our Compliance and Regulatory Affairs department, you will be responsible for assisting the Compliance and Regulatory Affairs Management in executing day-to-day tasks associated with managing, maintaining, and continually improving...

Job Title: Manager, Compliance and Regulatory AffairsImaging Endpoints is a leading Imaging Technology and Imaging Clinical Research Organization (iCRO) passionately focused on our vision to Connect Imaging to the CureTM. We are seeking a seasoned Manager, Compliance and Regulatory Affairs to join our team and contribute to our mission to customize each...