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Gardner Resources Consulting
Boston, MA, United States
Our Life Sciences client, located in the Greater Boston Area, is currently searching for a GCP Quality Assurance Contractor. The GCP Quality Assurance contractor will provide strategic leadership and direction for R&D Quality initiatives focused on Patient Advocacy, Marketing, HCP and Regulatory Affairs. The GCP Quality Assurance contractor will
Job Source: Gardner Resources ConsultingGardner Resources Consulting
Boston, MA, United States
Our Life Sciences client, located in the Greater Boston Area, is currently searching for a GCP Quality Assurance Contractor. The GCP Quality Assurance contractor will provide strategic leadership and direction for R&D Quality initiatives focused on Patient Advocacy, Marketing, HCP and Regulatory Affairs. The GCP Quality Assurance contractor will
Job Source: Gardner Resources ConsultingX4 Life Sciences
Boston, MA, United States
X4 Life Sciences are working with one of Boston's leading biotechs focusing on rare diseases across both small molecules & gene therapy programs. They're looking for a Director of GCP QA to facilitate their continued growth. This role is responsible for overseeing GCP activities and leading event investigations across a range of modalities. This i
Job Source: X4 Life SciencesVertex Pharmaceuticals
Boston, MA, United States
GCP Biomarker Quality Associate Director page is loaded GCP Biomarker Quality Associate Director Apply locations Boston, MA time type Full time posted on Posted 5 Days Ago job requisition id REQ-21957 Job Description General Summary: The Associate Director, Biomarker Operational Quality will provide biomarker q
Job Source: Vertex PharmaceuticalsRhythm Pharmaceuticals, Inc
Boston, MA, United States
Company Overview Rhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives of patients and their families living with rare neuroendocrine diseases. We develop medicines for previously untreatable or undertreated diseases and provide meaningful support for healthcare providers and patients and their families.
Job Source: Rhythm Pharmaceuticals, IncRhythm Pharmaceuticals
Boston, MA, United States
Company Overview Rhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives of patients and their families living with rare neuroendocrine diseases. We develop medicines for previously untreatable or undertreated diseases and provide meaningful support for healthcare providers and patients and their families
Job Source: Rhythm PharmaceuticalsRhythm Pharmaceuticals
Boston, MA, United States
Company Overview Rhythm is a global, commercial-stage biopharmaceutical company committed to transforming the lives of patients and their families living with rare neuroendocrine diseases. We develop medicines for previously untreatable or undertreated diseases and provide meaningful support for healthcare providers and patients and their families.
Job Source: Rhythm PharmaceuticalsAura Biosciences
Boston, MA, United States
Job Description Job Description Salary: About Aura Biosciences Aura Biosciences is a clinical- stage biotechnology company developing precision immunotherapies to treat solid tumors designed to preserve the function of the organ with cancer. Our lead candidate bel-sar is in late-stage clinical development for the treatment of patients with primary
Job Source: Aura BiosciencesCambridge, MA, United States
The Opportunity:
We are seeking a Quality professional to be a cornerstone to a growing and evolving Quality function at Relay Tx. You will partner with your Clinical Development colleagues to oversee several external contract vendors while simultaneously contributing and influencing the build of the Quality Management System as the team evolves along with our pipeline. This is a "wear many hats" role and an exciting opportunity for someone who enjoys the build. At Relay Tx, we take Quality seriously, but we don't take ourselves too seriously. You'll have fun in our collaborative and energetic environment where you'll face new challenges every day.
Your Role:
You will be front and center, serving as Relay Tx's primary Quality contact for external clinical and patient safety vendors.
You will contribute to the development of the GCP/GCLP/GVP Quality Management Systems, conduct risk assessments and identify areas to be audited and potential process improvements.
You will review and approve all things GCP/GCLP/GVP; study protocols and manuals, clinical study reports, investigator brochures, informed consent forms, safety management plans, aggregate reports, etc.
You will create and execute risk-based clinical trial audit plans and participate in clinical vendor evaluation and qualification.
You will create and implement a GCP/GCLP/GVP inspection readiness strategy and plan in collaboration with your Clinical Development colleagues
You will conduct internal audits and provide audit metrics, audit observations, and develop robust CAPAs for cross functional team and management review.
You will develop and execute Quality Agreements with applicable vendors.
You will interpret and manage quality investigations associated with GCP/GCLP/GVP operations.
You will be proactive, and you will effectively communicate with GCP/GCLP/GVP vendors to address and resolve complex and routine activities while building positive client/vendor relationships, fostering continuous improvement, and adding value to the Clinical Development team.
You will be flexible and adaptable. You will eagerly contribute to the development of the Quality Management System even in aspects that extend beyond GCP/GCLP/GVP, including maintaining and reviewing metrics to monitor performance.
You will provide Quality Assurance subject matter expertise, leadership, and guidance to external CROs as well as in support of your Relay Clinical Development colleagues.
You will provide review of applicable GCP/GCLP/GVP documentation and regulatory submissions.
You will contribute significantly to other areas of Quality Assurance as needed as Relay's Quality team grows and the QMS evolves.
Competencies for Success:
You have a keen attention to detail but can stay focused on the big picture of continual improvement.
You are a team-player, flexible and easy to work with in a fast and collaborative environment. You are solution oriented with a customer service approach.
You are willing to "roll up your sleeves" and engage in all aspects of the role, big and small.
You have great communication skills and don't mind showing them off by traveling to GCP/GCLP/GVP sites, domestic and international, and being the Quality ambassador of Relay Tx.
Your Background:
Bachelor's degree in a scientific field.
Minimum of 10+ years of Quality Assurance/GCP/GCLP/GVP Operations experience in pharmaceutical or biotech industry.
In-depth knowledge of GCP/GCLP/GVP and QA principles, practices, and standards; thorough understanding of FDA, MHRA, EMA and ICH quality regulations.
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About Relay Therapeutics
Relay Therapeutics is a clinical-stage precision medicines company transforming the drug discovery process with the goal of bringing life-changing therapies to patients. Built on unparalleled insights into protein motion and how this dynamic behavior relates to protein function, we aim to effectively drug protein targets that have previously been intractable, with an initial focus on enhancing small molecule therapeutic discovery in targeted oncology. Our Dynamo platform integrates an array of leading-edge experimental and computational approaches to provide a differentiated understanding of protein structure and motion to drug these targets. We have built a world-class team of leading experts from each of these disciplines, and they are driven by a deep collaboration at every step of our drug discovery process.
Our team is equal parts fearless and relentless, with a shared passion for working collaboratively in intellectually stimulating environments. If you're excited by the challenge of putting protein motion at the heart of drug discovery and passionate about making a difference in the lives of patients, join us!
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Email Alert for Associate Director, Quality Assurance (GCP) jobs in Cambridge, MA, United States
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You can always manage your preferences and update your interests to ensure you receive the most relevant opportunities.
Get ready to discover your next great opportunity.