Temporary QA Associate
To see similar active jobs please follow this link: Remote Development jobs
Who We Are
Vial is a global tech-driven CRO providing next-generation clinical trial management services. The Vial CRO powers its drug discovery arm, Battery Bio, an AI-powered hyper scalable biotech. Battery Bio harnesses Vial's unique 90% lower cost structure to produce more affordable drug development with efficient, streamlined clinical trials.
Our mission is to reimagine the drug discovery process to empower scientists to cure all human disease. We have assembled a talented team of clinical operators, chemists, and innovative thinkers to achieve this vision.
Vial is a San Francisco, California-based company founded by Simon Burns in October 2020. Since our founding, we have become a fast-growing company of 100+ employees with over $100 million in funding from esteemed investors including General Catalyst, Box Group, and Byers Capital.
Vial is rebuilding the infrastructure to advance research. By deploying technology at every step, we are creating a more efficient future for drug discovery.
What You'll Do
The Clinical QA Associate will be responsible for the execution and oversight of GCP QA activities related to clinical trials. This involves working closely with Clinical Operations, Engineering, IT and other supporting areas/development teams to assure management in accordance with FDA regulations, ICH-GCP, SOPs, and all other applicable regulations.
Duration:
01 May - 01 September
Travel:
Expected (25%-50%)
Responsibilities
Lead qualification, routine and for-cause audits of vendors & investigator sites to assess effectiveness of their QMS and compliance to GCP, approved clinical study protocols and contracts
Conduct Trial Master File (TMF) audits
Conducts internal audits (systems, processes, vendors, computer system validation)
Communicates audit findings to audit stakeholders for visibility, as well as collaborating with auditees to ensure appropriate implementation of Corrective and Preventive Action Plans (CAPAs), addressing root causes
Maintains databases for Investigator Site audit observations and CAPAs; Tracks, reviews, approves, and assesses the adequacy of CAPAs. Provides input and supports observation and CAPA tracking for external Clinical vendors.
Collaborates with sponsors, vendors, and investigator sites to provide QA support and oversight to clinical studies while assessing compliance with local regulations, GCP/ICH requirements, and SOPs
Implement Clinical QA plans to meet GCP quality standards, policies, and procedures
Support continuous improvement activities
Support oversight/execution of training program to ensure appropriate training of all staff
Provide Quality oversight to deviation/Quality Incident investigations including root cause analysis and CAPA development and follow through
Perform other related duties as assigned
Requirements
5+ years of experience in a pharmaceutical/biotech or CRO industry. Start-up experience preferred
Expert knowledge and understanding of ICH GCP and worldwide applicable regulatory requirements
Experience conducting internal, vendor and investigator site audits
Experience with software implementation
Strong organizational skills, ability to multi-task, attention to detail, self-starter, ability to prioritize
Excellent verbal, written communication, and presentation skills
$50 - $60 an hour
Why You’ll Love Working At Vial
Innate curiosity. At our core, we embody an insatiable curiosity. Our journey into the realm of clinical trials was ignited by a firsthand understanding of the challenges involved. This innate curiosity drives us to constantly innovate, seek fresh ideas, and bring our vision of reimagining clinical trials to life.
Fostering autonomy. Autonomy is our guiding principle. We firmly believe that when team members are entrusted with autonomy, they unleash their true potential. Our culture fosters an environment where each individual takes ownership of their domain, empowering them to make a profound impact.
The pursuit of mastery. We are dedicated to cultivating mastery. We understand the value of honing expertise in a craft. The pursuit of mastery, coupled with a deep sense of pride in one's workmanship, fuels our unwavering commitment to tackle intricate challenges. At Vial, we foster a culture of highly autonomous professionals, each an expert in their field, collaborating on an immensely demanding endeavor together.
Move fast, stay humble. Our strength lies in agility and humility. We firmly believe that intellectual honesty and a nimble mindset are the pillars of success. By staying adaptable and open-minded to all solutions, we tackle obstacles head-on, remaining humble in the face of adversity. This enables us to surmount the hurdles that confront us at every twist and turn.
Benefits (Not applicable to Contract or Temp Positions)
Competitive Equity Compensation
Health, Dental, and Vision Benefits
401k or RRSP Plan with Company Matching after first 90 days of employment
One time, Remote Office Setup Stipend
Robust Paid Parental Leave
Remote-First, Flexible Work Schedule
Unlimited Vacation
Temporary QA Associate
To see similar active jobs please follow this link: Remote Development jobs
Who We Are
Vial is a global tech-driven CRO providing next-generation clinical trial management services. The Vial CRO powers its drug discovery arm, Battery Bio, an AI-powered hyper scalable biotech. Battery Bio harnesses Vial's unique 90% lower cost structure to produce more affordable drug development with efficient, streamlined clinical trials.
Our mission is to reimagine the drug discovery process to empower scientists to cure all human disease. We have assembled a talented team of clinical operators, chemists, and innovative thinkers to achieve this vision.
Vial is a San Francisco, California-based company founded by Simon Burns in October 2020. Since our founding, we have become a fast-growing company of 100+ employees with over $100 million in funding from esteemed investors including General Catalyst, Box Group, and Byers Capital.
Vial is rebuilding the infrastructure to advance research. By deploying technology at every step, we are creating a more efficient future for drug discovery.
What You'll Do
The Clinical QA Associate will be responsible for the execution and oversight of GCP QA activities related to clinical trials. This involves working closely with Clinical Operations, Engineering, IT and other supporting areas/development teams to assure management in accordance with FDA regulations, ICH-GCP, SOPs, and all other applicable regulations.
Duration:
01 May - 01 September
Travel:
Expected (25%-50%)
Responsibilities
Lead qualification, routine and for-cause audits of vendors & investigator sites to assess effectiveness of their QMS and compliance to GCP, approved clinical study protocols and contracts
Conduct Trial Master File (TMF) audits
Conducts internal audits (systems, processes, vendors, computer system validation)
Communicates audit findings to audit stakeholders for visibility, as well as collaborating with auditees to ensure appropriate implementation of Corrective and Preventive Action Plans (CAPAs), addressing root causes
Maintains databases for Investigator Site audit observations and CAPAs; Tracks, reviews, approves, and assesses the adequacy of CAPAs. Provides input and supports observation and CAPA tracking for external Clinical vendors.
Collaborates with sponsors, vendors, and investigator sites to provide QA support and oversight to clinical studies while assessing compliance with local regulations, GCP/ICH requirements, and SOPs
Implement Clinical QA plans to meet GCP quality standards, policies, and procedures
Support continuous improvement activities
Support oversight/execution of training program to ensure appropriate training of all staff
Provide Quality oversight to deviation/Quality Incident investigations including root cause analysis and CAPA development and follow through
Perform other related duties as assigned
Requirements
5+ years of experience in a pharmaceutical/biotech or CRO industry. Start-up experience preferred
Expert knowledge and understanding of ICH GCP and worldwide applicable regulatory requirements
Experience conducting internal, vendor and investigator site audits
Experience with software implementation
Strong organizational skills, ability to multi-task, attention to detail, self-starter, ability to prioritize
Excellent verbal, written communication, and presentation skills
$50 - $60 an hour
Why You’ll Love Working At Vial
Innate curiosity. At our core, we embody an insatiable curiosity. Our journey into the realm of clinical trials was ignited by a firsthand understanding of the challenges involved. This innate curiosity drives us to constantly innovate, seek fresh ideas, and bring our vision of reimagining clinical trials to life.
Fostering autonomy. Autonomy is our guiding principle. We firmly believe that when team members are entrusted with autonomy, they unleash their true potential. Our culture fosters an environment where each individual takes ownership of their domain, empowering them to make a profound impact.
The pursuit of mastery. We are dedicated to cultivating mastery. We understand the value of honing expertise in a craft. The pursuit of mastery, coupled with a deep sense of pride in one's workmanship, fuels our unwavering commitment to tackle intricate challenges. At Vial, we foster a culture of highly autonomous professionals, each an expert in their field, collaborating on an immensely demanding endeavor together.
Move fast, stay humble. Our strength lies in agility and humility. We firmly believe that intellectual honesty and a nimble mindset are the pillars of success. By staying adaptable and open-minded to all solutions, we tackle obstacles head-on, remaining humble in the face of adversity. This enables us to surmount the hurdles that confront us at every twist and turn.
Benefits (Not applicable to Contract or Temp Positions)
Competitive Equity Compensation
Health, Dental, and Vision Benefits
401k or RRSP Plan with Company Matching after first 90 days of employment
One time, Remote Office Setup Stipend
Robust Paid Parental Leave
Remote-First, Flexible Work Schedule
Unlimited Vacation