Associate Director, Clinical Quality Assurance
3 weeks ago
Who we are
Abdera Therapeutics Inc. is a precision oncology company developing next-generation targeted radiation therapies- one of the most cutting-edge and highly promising areas of drug development. The company is built on a proprietary modular technology platform optimized for the delivery of radioisotopes to selectively destroy tumor cells while sparing healthy cells. Abdera is using this platform to enable the rapid development of a broad range of safe and efficacious therapies serving cancer patients with limited treatment options.
Abdera Therapeutics is growing rapidly and seeking key new team members who thrive at the cutting-edge of innovation. Come join us and be a part of the ground-breaking team set to unlock the power of targeted radiotherapy
What we look for
At Abdera Therapeutics, we are looking for curious and committed individuals who are ready for the opportunity to transform the way people living with cancer can be treated. We are relentless in our focus to offer new hope to families facing devastating diagnoses. We are in search of team members who work collaboratively with a diverse group of colleagues, respectfully engaging one another while collectively and inclusively tackling any challenges we may face. We are building an exciting and fast paced company passionate about discovering and developing tomorrow’s most innovative cancer therapies.
Abdera is seeking an Associate Director, Clinical Quality Assurance, to lead clinical quality for Abdera’s novel oncology therapy clinical programs. The Associate Director of Clinical Quality Assurance will be responsible for building the clinical quality assurance processes and providing quality oversight for the clinical programs and CRO throughout the development stages of antibody-based radiopharmaceuticals. This position provides cross-functional GMP/GCP/GLP compliance support for ongoing and new clinical studies.
Salary Range: US$ 155K – 190K
Principal Responsibilities
Provide quality oversight to CROs and CSPs
- Provide CQA oversight to Phase I-III global clinical studies to ensure study conduct compliance in accordance with GCP and applicable regulatory requirements.
- Participates in clinical programs and coordinates the cQA interface with Contract Clinical Research Organizations (CROs), Contract Service Providers (CSPs), Bioanalytical Labs and Investigator Sites. Conduct QA review of clinical protocols, ICFs, Clinical Investigator's Brochure, Clinical Study Report audits and other clinical trial specific documents.
- Provide guidance for investigations as well as corrective and preventive action (CAPA) plans for compliance issues and/or observations.
- Collaborate with clinical operations study leads to ensure Sponsor Oversight is maintained, documented, and improved in ongoing clinical programs.
- Compile and communicate compliance related metrics, risks, and compliance challenges to teams and management.
- Schedule and oversee CRO/CSP qualification and routine and non-routine quality assurance audits to include clinical investigator sites, CROs/CSPs, process, system, study project and document.
- Ensure inspection readiness preparation with CROs, CSPs, clinical sites, as applicable.
Support Clinical Programs
- Guide Clinical team in the development of Clinical SOPs and other quality documents.
- Work closely with GxP Quality Assurance and functional areas responsible for the conduct of clinical research (e.g., Clinical Operations, Clinical Development, Biostatistics and Data Management, Pharmacovigilance, etc.)
- Recommend and lead the implementation of quality initiatives to ensure clinical compliance to global regulatory requirements (e.g., US FDA, EMA, etc.)
- Supports regulatory inspections of the company and its clinical vendors as needed.
- Provides cQA support for safety related monitoring and pharmacovigilance.
- Identification of investigator sites that may pose a risk to that portfolio, conducting regular investigator site audits and management of subsequent corrective and preventive actions plans (CAPA).
Support building the overall Quality Management Systems
- Establishes, refines, implements, and maintains cQA systems, policies, and procedures for oversight of the Abdera’s clinical operations.
- Ensures implementation of a risk-based approach to regulatory compliance.
- Supports the organization's training program as it relates to GCP and clinical compliance.
Qualifications & Experience
- Minimum of a master’s degree in life science or equivalent and 10+ years' experience in GXP and Quality Systems in biotechnology or pharmaceutical environment.
- Demonstrated in-depth experience of establishing, refining, and operating Clinical Quality Assurance related systems in the Biotechnology industry.
- In depth knowledge of regulations and guidance supporting GCP and GLP to include FDA, EMA, ISO standards and ICH guidelines with direct impact to clinical programs.
- Experience reviewing and collaborating on regulatory submissions as well as hosting inspections/interactions.
- Experience working effectively with CROs/CSPs.
- Experience with electronic Quality Management Systems and Trial Master File.
Skills and Abilities
- A solid understanding of GCP, GLP, GMPs and CMC requirements is expected.
- Strong knowledge of Quality, Compliance, US & International cGxPs, regulations, product development and manufacturing.
- Must be familiar with ICH regulations and FDA/EMA requirements and expectations, plus experience with health authority inspections.
- Demonstrated thought leadership in clinical Quality Assurance.
- Experience in preparing regulatory filings.
- Strong interpersonal and collaboration skills.
- Excellent verbal and written communication skills.
- Ability to operate in a fast-paced, multi-disciplinary industrial environment.
- Ability to critically evaluate and troubleshoot complex problems and attention to detail.
Abdera is an equal opportunity employer that is committed to diversity and inclusion in the workplace. At Abdera, we prohibit harassment of any kind and any form of discrimination including but not limited to discrimination based on race, color, sex, religion, marital status, sexual orientation, national origin, disability, veteran status, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.
This is applicable to all employment practices within our organization, including hiring, recruiting, promotion, termination, layoff, recall, leave of absence, compensation, benefits, training, and apprenticeship.
Powered by JazzHR
42eUzp7SXM
-
Associate Director, Clinical Quality Assurance
4 weeks ago
South San Francisco, United States Remegen Biosciences, Inc. Full timeJob DescriptionJob DescriptionORGANIZATIONRemeGen Biosciences is a biopharmaceutical company, focusing on the discovery and development of innovative medicines for the treatment of cancer and autoimmune diseases, based in South San Francisco, California, and Rockville, Maryland. By leveraging our deep insights into oncology and immunology, advanced protein...
-
Associate Director, Clinical Quality Assurance
4 weeks ago
South San Francisco, United States RemeGen Biosciences Full timeORGANIZATIONRemeGen Biosciences is a biopharmaceutical company, focusing on the discovery and development of innovative medicines for the treatment of cancer and autoimmune diseases, based in South San Francisco, California, and Rockville, Maryland. By leveraging our deep insights into oncology and immunology, advanced protein engineering/design...
-
Associate Director, Clinical Quality Assurance
3 weeks ago
South San Francisco, United States Remegen Biosciences, Inc. Full timeJob DescriptionJob DescriptionORGANIZATIONRemeGen Biosciences is a biopharmaceutical company, focusing on the discovery and development of innovative medicines for the treatment of cancer and autoimmune diseases, based in South San Francisco, California, and Rockville, Maryland. By leveraging our deep insights into oncology and immunology, advanced protein...
-
South San Francisco, United States Planet Pharma Full timePosition Summary Our client seeks a Quality Assurance (QA) Director/Senior Director to lead the company’s clinical Quality Assurance (cQA) program. The incumbent will assist in the development of quality systems to ensure clinical trials are conducted in accordance with appropriate regulations, guidelines, procedures, and protocols. The incumbent is also...
-
Director, Clinical Quality Assurance
4 weeks ago
South San Francisco, United States Alumis Inc. Full timeAlumis Inc. is a precision medicines company with the mission to transform the lives of patients with autoimmune diseases. Even with treatment innovations of the last two decades, many patients with immunologic conditions continue to suffer - our goal is to fundamentally change the outcomes for these patients. Alumis is hiring a Clinical Quality Assurance...
-
Director, Clinical Quality Assurance
2 weeks ago
South San Francisco, United States Alumis Inc. Full timeAlumis Inc. is a precision medicines company with the mission to transform the lives of patients with autoimmune diseases. Even with treatment innovations of the last two decades, many patients with immunologic conditions continue to suffer - our goal is to fundamentally change the outcomes for these patients. Alumis is hiring a Clinical Quality Assurance...
-
Director, Clinical Quality Assurance
3 weeks ago
South San Francisco, United States Alumis Inc. Full timeAlumis Inc. is a precision medicines company with the mission to transform the lives of patients with autoimmune diseases. Even with treatment innovations of the last two decades, many patients with immunologic conditions continue to suffer - our goal is to fundamentally change the outcomes for these patients. Alumis is hiring a Clinical Quality Assurance...
-
Director, Clinical Quality Assurance
3 weeks ago
South San Francisco, California, United States Alumis Inc. Full timeAlumis Inc. is a precision medicines company with the mission to transform the lives of patients with autoimmune diseases. Even with treatment innovations of the last two decades, many patients with immunologic conditions continue to suffer - our goal is to fundamentally change the outcomes for these patients.Alumis is hiring a Clinical Quality Assurance...
-
Director, Clinical Quality Assurance
4 weeks ago
South San Francisco, California, United States Alumis Inc. Full timeAlumis Inc. is a precision medicines company with the mission to transform the lives of patients with autoimmune diseases. Even with treatment innovations of the last two decades, many patients with immunologic conditions continue to suffer - our goal is to fundamentally change the outcomes for these patients.Alumis is hiring a Clinical Quality Assurance...
-
Director, Clinical Quality Assurance
2 months ago
South San Francisco, California, United States Alumis Inc. Full timeAlumis Inc. is a precision medicines company with the mission to transform the lives of patients with autoimmune diseases. Even with treatment innovations of the last two decades, many patients with immunologic conditions continue to suffer - our goal is to fundamentally change the outcomes for these patients.Alumis is hiring a Clinical Quality Assurance...
-
Director, Clinical Quality Assurance
1 month ago
South San Francisco, United States Alumis Full timeJob DescriptionJob DescriptionSalary: Alumis Inc. is a precision medicines company with the mission to transform the lives of patients with autoimmune diseases. Even with treatment innovations of the last two decades, many patients with immunologic conditions continue to suffer - our goal is to fundamentally change the outcomes for these patients. Alumis is...
-
Director, Clinical Quality Assurance
3 weeks ago
South San Francisco, United States Alumis Full timeJob DescriptionJob DescriptionSalary: Alumis Inc. is a precision medicines company with the mission to transform the lives of patients with autoimmune diseases. Even with treatment innovations of the last two decades, many patients with immunologic conditions continue to suffer - our goal is to fundamentally change the outcomes for these patients. Alumis is...
-
South San Francisco, United States Annexon Full timeWork Location Corporate Headquarters (South San Francisco, CA) – Hybrid Position Summary Annexon Biosciences seeks a Quality Assurance (QA) Director/Senior Director to lead the company's clinical Quality Assurance (cQA) program. The incumbent will assist in the development of quality systems to ensure clinical trials are conducted in accordance with...
-
South San Francisco, United States Annexon Full timeWork Location Corporate Headquarters (South San Francisco, CA) – Hybrid Position Summary Annexon Biosciences seeks a Quality Assurance (QA) Director/Senior Director to lead the company's clinical Quality Assurance (cQA) program. The incumbent will assist in the development of quality systems to ensure clinical trials are conducted in accordance with...
-
South San Francisco, United States Planet Pharma Full timePosition SummaryOur client seeks a Quality Assurance (QA) Director/Senior Director to lead the company’s clinical Quality Assurance (cQA) program. The incumbent will assist in the development of quality systems to ensure clinical trials are conducted in accordance with appropriate regulations, guidelines, procedures, and protocols.The incumbent is also...
-
South San Francisco, United States Annexon, Inc. Full timeWork Location Corporate Headquarters (South San Francisco, CA) – Hybrid Position Summary Annexon Biosciences seeks a Quality Assurance (QA) Director/Senior Director to lead the company's clinical Quality Assurance (cQA) program. The incumbent will assist in the development of quality systems to ensure clinical trials are conducted in accordance with...
-
South San Francisco, United States Annexon, Inc. Full timeWork Location Corporate Headquarters (South San Francisco, CA) – Hybrid Position Summary Annexon Biosciences seeks a Quality Assurance (QA) Director/Senior Director to lead the company's clinical Quality Assurance (cQA) program. The incumbent will assist in the development of quality systems to ensure clinical trials are conducted in accordance with...
-
Senior Director GCP Quality Assurance
3 days ago
South San Francisco, United States Meet Full timeMy client is an exciting biopharmaceutical company advancing therapies for classical complement-mediated neuroinflammatory diseases. They are are seeking a Quality Assurance Director/Senior Director to lead their clinical Quality Assurance (cQA) program. This role involves developing and managing quality systems to ensure clinical trials comply with...
-
Senior Director GCP Quality Assurance
5 days ago
South San Francisco, United States Meet Full timeMy client is an exciting biopharmaceutical company advancing therapies for classical complement-mediated neuroinflammatory diseases. They are are seeking a Quality Assurance Director/Senior Director to lead their clinical Quality Assurance (cQA) program. This role involves developing and managing quality systems to ensure clinical trials comply with...
-
Director, Quality Assurance
4 weeks ago
South San Francisco, United States Cellares Full timeWe are seeking a highly motivated collaborative Director of Quality Assurance for our South San Francisco location to develop, establish, implement and maintain a phase appropriate cGMP Quality management system for the Cell & Gene Therapy operations to support pre-clinical and clinical manufacturing. This individual will be responsible to lead and grow the...
