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The successful candidate will combine strong laboratory and scientific expertise with the ability to manage study activities, solve technical problems, communicate effectively with Sponsors, and deliver high-quality work within a regulated CRO environment. The Associate Senior Scientist performs advanced scientific activities supporting study delivery, method development and validation, data analysis, troubleshooting, and client-focused technical solutions.

Alliance Pharma Inc

Associate Sr. Scientist- LCMS

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Review, approve investigations, Root Cause Analysis (RCA), Corrective Action Prevention (CAPA) and Effectiveness Check (EC) plans and track till closure for quality events arising from Audits; and from Quality Issues, Inspections or during similar QA activities as assigned. May perform pre-inspection visits at sites, host audits/inspections; ensure proper conduct of customer-initiated audits and mock regulatory inspections, and assist in regulatory facility inspections, as assigned.

YEAR

IQVIA Holdings Inc

Senior QA Auditor - GCP Audits

When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration. Medical record and research source documentation verification against case report form data, working with site staff to resolve issues, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements.

Medpace, Inc.

Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)

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The position will require strong oversight for patient safety issues that arise at both the individual and aggregate levels within the company and in collaboration with co-development and business partners strong decision-making skills on all issues involving safety assessment and surveillance responsibility for compliant timely and complete regulatory authority engagement with particular emphasis on benefit-risk assessments and risk identificationcharacterization and mitigationmanagement and effective communication of safety information to internal and external stakeholders. Through the discovery development and commercialization of proprietary therapeutics Incyte has established a portfolio of first-in-class medicines for patients and a strong pipeline of products in Hematology Oncology and Inflammation and Autoimmunity Headquartered in Wilmington Delaware Incyte has operations in North America Europe and Asia.

Investigator Jobs in Cherry Hill, NJ

Associate Sr. Scientist- LCMS Alliance Pharma Inc

Senior QA Auditor - GCP Audits IQVIA Holdings Inc

Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate) Medpace, Inc.

Senior Medical Director - Executive Medical Director, Global Risk Management & Safety Surveillance Incyte Corp

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