PV Scientist: Lead Safety Data Reviews & Reporting
TechDigital Group
An established industry player is seeking a dedicated professional to join their Worldwide Patient Safety group. This role involves supporting Medical Safety Assessment Physicians in leading Safety Data Review Teams, conducting signal detection activities, and ensuring compliance with pharmacovigilance regulations. You will have the opportunity to collaborate across functions and contribute to critical safety reports. If you are passionate about patient safety and have a strong background in the pharmaceutical industry, this position offers a chance to make a meaningful impact in drug development and safety management. #J-18808-Ljbffr TechDigital Group
- ...Description The Worldwide Patient Safety group is responsible for... ...safety monitoring, safety reporting, contribution to benefit-... ...Physicians (MSAP) in leading Safety Data Review (SDR) Teams. Appropriately... ...and contribute to specified PV sections of the Periodic Benefit...DataWorldwide
- ...development, regulatory, and safety to continually assess and analyze clinical safety signal data and inform key stakeholders to... ...medical affairs, independent review committees, and regulatory authorities... ...ensure timely identification, reporting, and response to health...DataLocal areaImmediate start
$94.4k - $266.3k
You Are: A senior Oracle Utilities reporting strategist who brings the vision... ...translate into Oracle Utilities data models and reporting architectures. You lead with strategy — designing frameworks... ..., quality standards, and review cadences. Engage client business...DataWork experience placementWork at officeLocal area- ...years of experience in archaeological project supervision, with duties including supervising fieldwork, authoring reports, and analyzing archaeological data. This role offers the potential for remote work and involves collaboration on various public and private projects...DataRemote job
- A pharmaceutical company is seeking an experienced Pharmacovigilance Scientist in Berkeley Heights, NJ. This role involves performing safety data reviews, leading aggregate reporting, and ensuring compliance with safety regulations. Candidates should have an advanced degree...Data
$124k - $170k
...experienced Pharmacovigilance Scientist to join our Drug Safety and Pharmacovigilance team. Reporting to the Associate... ...and assessed. The PV Scientist will play a... ...in cumulative safety data reviews, safety surveillance,... ..., literature reviews. Lead aggregate report (PSUR...DataTemporary workLocal areaFlexible hours- ...of workplans, conducting field work, and writing summary reports, to final remedial documents Field work will include... ...accordance with ASTM E1527. Prepare summary reports including reviewing laboratory analytical data; interpreting and tabulating data and preparing tables;...DataWork experience placementFor subcontractorWork at office
- ...global talent solutions firm in New Jersey is seeking a professional for a key role in medical writing and clinical safety. You will analyze clinical safety data and collaborate with global health authorities. A minimum of 2 years in medical or technical writing is required...DataWork at office
$178.5k - $257.83k
Job title: Global Periodic Reporting lead Location: Cambridge, MA / Morristown, NJ / Swiftwater, PA About the Job Join the engine of Sanofi... ...develop robust , compliant, and controlled processes for Periodic Safety Report (PSR) authoring and vendor oversight. You will lead the...Full timeWorldwide- ...Senior Clinical Scientist Location: Cambridge, MA... ...through clinical study report completion, in full compliance... ...to CRF design and review completion instructions... ...Review and analyze data listings, patient profiles... ...to the CRD and Project Lead Partner with Clinical...Data
- ...Clinical Research Physician, Clinical Operations, Data Management, Statistics, Drug Safety, Regulatory and Project Management. Review and query of hematology/oncology data... ...as appropriate). Assist with clinical study report preparation to include narrative writing Participate...DataPermanent employmentContract workWork at officeImmediate start
- ...Complaints Regulatory Reporting Lead The Complaints Regulatory Reporting Lead is a key analytical role that globally sits at the intersection... ...operations, business insights, regulatory compliance, and data strategy. This role owns the design and delivery of complaint...DataLocal area
$71.91k - $87.14k
...term commitment, we are leading the way to unlock the... ...Therapy team.The Associate Scientist/Engineer is responsible... ...leading investigation reports in support of S12 CAR T... ...as author or technical reviewer of departmental... ...inspections.* Knowledge of data trending and tracking,...DataHourly payFull timeTemporary workPart timeFor contractorsWork experience placementSummer workLive inWork at officeLocal areaRemote workMonday to FridayFlexible hoursShift workWeekend workDay shift- ...CLIA General Supervisor, the Lead Medical Laboratory Scientist performs specimen... ...moderate complexity testing, and reports accurate results.... ...previous results as applicable. Reviews final reports for accuracy... ...dates of all supplies. Safety: Demonstrates knowledge and...Hourly payFull timeTemporary workPart timeFor contractorsFor subcontractorFlexible hoursShift work
$119.7k - $222.3k
...Principal Clinical Data Scientist Imagine shaping the data that brings... ...assigned trials. You will lead end-to-end data management activities... ...design, analysis, or reporting outcomes. Collaborate... ...upon joining Novartis will be reviewed periodically. Novartis may change...DataWorldwide- ...May serve as Clinical Trial Lead for one or more trials. May lead... ...meetings. Conduct literature reviews. Submit clinical documents to... ...narratives. Monitor clinical data for trends. Develop data... ...documents (IB, DSUR, PSUR, orphan reports, HA, EC, IRB responses). Contribute...DataFlexible hoursShift work
$173.39k - $210.11k
...serve as Clinical Trial Lead for one or more trials... ...required Conduct literature review Submit clinical... ...narratives Monitor clinical data for specific trends... ...contributions to clinical study reports (CSRs) and clinical... ..., Global Clinical Scientist - Psychiatry #J-18808-...DataHourly payFull timeTemporary workPart timeSummer workFlexible hoursShift work$173.39k - $210.11k
...Manager, Global Clinical Scientist - PsychiatryMadison -... ...serve as Clinical Trial Lead for one or more trials*... ...* Conduct literature review* Submit clinical documents... ...* Monitor clinical data for specific trends* Develop... ...to clinical study reports (CSRs) and clinical portions...DataHourly payFull timeTemporary workPart timeFor contractorsSummer workLive inWork at officeLocal areaRemote workFlexible hoursShift work$152k - $190k
...of experience in the P&C industry. This role involves leading the production of all reserving reporting, both internally for management and externally for... ...should have strong skills in financial reporting and data management processes, with a background in leading reporting...Data$201.84k - $302.76k
Director, Clinical Safety Scientist Job Requisition ID: 1768 Posting Start... ...with product safety leads. This position proactively creates... ...integrates and analyzes safety data from multiple sources to deliver... ...and aggregate safety reports. Project Management: Serves as...Data- ...relationships with IFM suppliers, reports to the Head of IFM & Workplace... ...Services delivery.This role leads strategic supplier... ...Experience, and Technology, creating data-driven solutions that combine... ...messagingConduct regular IFM contract reviews to assess effectiveness, share...DataContract workTemporary workWork at officeImmediate startRelocation3 days per week
- Senior Demand Lead Location: Morristown, NJ Hybrid Work Schedule... ...Demand Planners to ensure accurate data reflecting business needs and... ..., launches, and periodically review planning master data to ensure... .... Analyze IBP dashboards and reporting tools to track performance...DataTemporary work
- Job Title: Demand Lead Location: Morristown, NJ Hybrid Work Schedule... ...Planners to ensure accurate data to reflect business needs and... .... As well periodically review planning master data to ensure... .... Analyze IBP dashboards and reporting tools to track performance against...DataTemporary work
$100.5k - $145.17k
Job Title: Clinical Real World Data Scientist/Methodologist Join the team... ...reliable, trustworthy, and timely. Lead and execute feasibility... ...g., clinical scores, patient‑reported outcomes) from EHR systems, including... ...standards (sourced from peer‑reviewed references such as PubMed,...Data$148.5k - $214.5k
Job title: Clinical Scientist, Ophthalmology Location:... ...(CRD) and/or clinical leads to ensure scientific management... ...and clinical case review of study data, review of study plans and draft study reports/publications for... ...and investigations of safety cases with the Clinical...DataFull time$130k - $165k
...execution, including document review, IND/CTA approval, etc. Your... ...CSRs, IMPDs, IBs, and annual reports to ensure content and format meet... ...Experience supporting and/or leading IND/CTA submissions Understanding... ...(Clinical Operations, Data Management, Biostatistics, and...DataLocal area$79.4k - $162.7k
...execution tools.* ### Analyze signaling and data plane components to identify potential... ...to the development of technical security reports.### ### **Qualifications:**### *Required*... ...driven by a higher purpose - to ensure the safety of our nation.**An environment of trust.*...DataContract workWork experience placementImmediate startFlexible hours$255.48k - $309.59k
...Market Access, and Patient Safety to move with urgency—... ...Medical Communications Lead is the Cell Therapy... ...cell therapy value chain. Reporting into the SVP, Head Cell... ...dissemination of data through publications, congresses... ...number so we can review. Communications related...DataHourly payFull timeTemporary workPart timeFor contractorsSummer workLive inWork at officeLocal areaRemote workWorldwideFlexible hoursShift work- ...QC Associate Scientist, Microbiology Location: Summit, NJ 07901 Assignment Duration: 06 months... ...to contract labs and track results/reports. Evaluate environmental/personnel monitoring... ...associated with Microbiological testing. Support data trending and tracking of results. Perform...DataContract workLocal areaShift workNight shiftRotating shift
$40.79 - $52.03 per hour
...Specific Requirements Adheres to safety policies regarding safe... ...dates in designated logs, records data received/placed into use of... ...action is needed, Periodically reviews policy/procedure/instrument... ...that all written/verbal reports are accurate/logicefore release...DataHourly payPart timeShift workNight shift
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