Senior Clinical Safety Data Analyst

We are seeking a highly skilled Safety Data Analyst to join our Expedited Safety Reporting team at Bristol Myers Squibb.As a Safety Data Analyst, you will play a critical role in ensuring the accuracy and quality of safety data related to expedited safety reports. You will be responsible for performing high-quality data entry of Individual Case Safety...

Job SummaryThe ideal candidate will possess a strong background in pharmacovigilance and safety data processing, with a focus on adverse event reconciliation. In this role, the Safety Data Analyst, Reconciliation Specialist will be responsible for reviewing and reconciling adverse event data in the Worldwide Patient Safety database and clinical trial...

At Statistics & Data Corporation (SDC), we are seeking a highly skilled Senior Clinical Data Specialist. This role will manage medical coding activities for multiple projects, including the coding of clinical terms, dictionary subscription management, and validation. The successful candidate will be responsible for ensuring medical coding practices are in...

**Clinical Database Expert Wanted**At Statistics & Data Corporation (SDC), we're seeking a highly skilled Senior Clinical Programmer to join our team of experts in clinical research and data management.The ideal candidate will have a strong background in database development and a deep understanding of clinical trials. As a Lead Database Developer, you will...

About ICON plcICON plc is a world-leading healthcare intelligence and clinical research organization.We foster an inclusive environment driving innovation and excellence, and we're committed to shaping the future of clinical development.Job Title: Senior Clinical Validation AnalystLocation: Chennai/Bangalore Office basedJob Summary:As a Senior Clinical...

Unlock your potential in a dynamic environment where collaboration and innovation thrive.About the Role:We are seeking a highly skilled Clinical Data Analyst II to join our team of experts in statistical programming. As a key member of our team, you will be responsible for analyzing and interpreting clinical study data, as well as developing and maintaining...

Enhancing Data Insights for Patient SafetyBristol Myers Squibb is a global biopharmaceutical company committed to transforming patient lives through innovative science and sustainable solutions. We are seeking a highly skilled Data Analytics Manager - Clinical and Safety to join our team and contribute to our mission.This role is responsible for developing...

Unlock the Potential of Your CareerBristol Myers Squibb is a global pharmaceutical company that transforms patients' lives through science. We are seeking a highly skilled Clinical Data Analyst to join our team and play a crucial role in biospecimen management.About the RoleThis is an exciting opportunity for a talented individual with experience in data...

Job Overview:Makro seeks a skilled Senior Clinical Pricing Analyst to lead the development and implementation of pricing strategies for clinical services. This role ensures the company maintains competitive and profitable pricing structures and supports the Request for Quotation (RFQ) and Request for Proposal (RFP) processes for clinical products and...

Job DetailsThis is a Medical Data Safety Specialist role where you will be part of the Pharmacological Department. Your key responsibility will be to report adverse effects and side effects, in accordance with current Dutch and European legislation for pharmacology.You may also train colleagues in departments such as marketing and sales, medical and clinical...

Transforming Patients' Lives through ScienceBristol Myers Squibb is a leading pharmaceutical company dedicated to transforming patients' lives through science. Our team of passionate and innovative professionals works tirelessly to develop cutting-edge treatments that make a real difference in people's lives.Job SummaryWe are seeking an experienced Senior...

Clinical Supplies IRT Business AnalystAs a Clinical Supplies IRT Business Analyst at MakroCare, you will play a pivotal role in bridging the gap between complex business processes and the product team. Your expertise will be crucial in ensuring the seamless integration of clinical supply chain management with Interactive Response Technology (IRT) and EDC...

**About MaxisIT Inc.**We are a leading provider of data services, and we're seeking an experienced Senior Statistical Programmer to join our team in Hyderabad.Salary: $120,000 - $180,000 per annum (dependent on experience)Job Description:The successful candidate will be responsible for handling TLF/ADaM data conversion, data validation, and clinical...

Job SummaryWe are seeking an Associate Safety Scientist to support the Expedited Safety Reporting team at Bristol Myers Squibb. As an Associate Safety Scientist, you will play a key role in ensuring the quality and integrity of safety data, working closely with safety scientists and medical review safety physicians to expedite the processing of SUSAR...

Company OverviewPharma Stuff, a leading pharmaceutical manufacturing company, is dedicated to innovation and quality in the production of life-saving drugs. With a strong presence in the Pharmaceutical Manufacturing industry, our firm employs over 1000 professionals focused on excellence. We promote growth by nurturing talented individuals from within our...

About LifelancerLifelancer is a talent hiring platform in Life Sciences, Pharma, and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech, data science, and IT domains.Job Title: Senior Clinical Validation AnalystLocation: Chennai/Bangalore Office-basedJob Responsibilities:Conduct activities in Rave SAS and...

Job Description:We are seeking a skilled Clinical Data Management Expert Lead to manage medical coding activities for multiple projects. The ideal candidate will have exceptional working knowledge of clinical trials and coding specialist roles in the drug development process.Key Responsibilities:Manage medical coding practices to ensure compliance with US...

DescriptionThe Worldwide Patient Safety group at Bristol Myers Squibb is responsible for ensuring the safety of our medicines. This includes all pharmacovigilance and pharmaco-epidemiology deliverables including single case and aggregate safety monitoring, safety reporting, contribution to benefit-risk assessment, risk management planning and strategy, and...

At Lifelancer, we are seeking a highly skilled Clinical Data Specialist I to join our team.About the RoleThe ideal candidate will be responsible for contributing to all aspects of global clinical trial activities, delivering study outcomes within schedule, budget, quality and performance standards. This role may lead specific aspects of global clinical...

Responsibilities:As a Clinical Coding Analyst at R1 RCM, you will be responsible for reviewing inpatient medical records and assigning accurate ICD-10-CM codes for diagnoses and procedures. You will also ensure the correct sequencing of codes based on medical record documentation and assign POA indicators correctly. Additionally, you will have a thorough...