Clinical Trial Associate

  • location: Cambridge, MA
  • type: Contract
  • salary: $85 - $94.26 per hour
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job description

Clinical Trial Associate

job summary:

  • Provide leadership and influence to the Company Clinical Compound Support QA Program Managers and partner with key stakeholders that are integral to clinical development activities.
  • Manage Therapeutic Area Programs of a highly complex nature and/or high risk programs including, multiple indications, data safety monitoring boards, endpoint review committees as well as those requiring the coordination of multiple vendors.
  • Serve as a strategic GCP quality resource providing GCP technical guidance recommendations to development teams
  • Maximize effectiveness and efficiency in the use of available resources in conducting clinical compound support quality assurance activities.

location: Cambridge, Massachusetts
job type: Contract
salary: $85.00 - 94.26 per hour
work hours: 9 to 5
education: Bachelors
  • Leadership & Partnership

    • Provide GCP QA leadership to drug development teams.
    • Act as a quality expert to provide GCP compliance interpretation, consultation, training, and recommendations.
    • Coach, educate and collaborate with external sites and cross functional Company staff in global regulatory readiness activities and responses in support of successful marketing applications.
  • Implementation of Audit and Compliance Programs

    • Lead domestic and international audits of sites, documents, databases, vendors or internal systems in compliance with the Code of Federal Regulations, local regulations, ICH and Company policies and procedures. Assess impact of audit findings on subject safety, data integrity, and business operations. Audits conducted require advanced auditing skills and may include the technically complex assignments, including audits of potentially high risk studies/vendors.
    • Ensure that investigator, vendor, facility and system audits are conducted, identified critical compliance risks are mitigated and communicated to Quality Assurance senior management, and that appropriate corrective/preventative action plans implemented.
    • Collaborate with Global Clinical Compound Support QA (CCS QA) and all related functional areas to ensure that clinical trial activities are conducted in compliance with Good Clinical Practice (GCP) regulations, the International Conference on Harmonization (ICH) and Company Policies and Procedures.
    • Develop and implement a strategic quality plan for assigned compounds.
    • Supervise and manage investigations into scientific misconducts and/or serious breach of GCP. Analyze findings to identify root/probable cause. Propose, document and track appropriate corrective actions. Assure reporting of potential or confirmed violations to regulatory authorities.
    • Assist Company R&D during GCP regulatory inspections. Provide GCP compliance technical support during inspections of investigator sites and Company facilities. Work with the stakeholders to ensure appropriate and timely response and follow-up.
    • Collaborate with QA Global Compound Compliance and Quality Systems to identify and mitigate GCP quality and compliance issues with potential impact across multiple compounds, sites, or functional groups including Company EU, Company Asia, and JDC (Japan Development Center).
    • Rapidly identify, evaluate, and escalate inadequate responses to CCS QA management
  • Report GCP Compliance status for Therapeutic Teams

    • Monitor compliance issues identified across clinical programs. Analyze audit program results, quality issues, and quality investigations in order to optimize global operations and overall global state of compliance.
    • Provide appropriate risk analysis for key stakeholders
    • Elevate systemic problems with appropriate recommendations/solutions to upper management for immediate and long-term resolution.
    • Report metrics for assigned compounds to QA management, clinical staff. Evaluate if CAPA(s) are required and monitor implementation.
  • Leverage Resources Efficiently and Effectively

    • Lead systems monitoring and process improvement initiatives that enhance regulatory compliance and CQA operating efficiency.
    • Ensure reports and corrective actions are developed and completed within timelines mandated in internal procedures.
    • Leverage global CCS QA Team to drive for on time deliverables and quality service delivery excellence.
  • B.S. in Science, Nursing, or related scientific field.
  • 7 years of experience in the pharmaceutical or biotechnology industry with 5 years of GCP-related Quality Assurance experience.
  • In Depth knowledge of the applicable global GCP regulations, Good Clinical Practices, ICH Guidelines
  • Advanced knowledge in the conduct and reporting of audits and the translation of findings into corrective actions plans that mitigate risks to the company, to safety and data integrity.
  • Strong knowledge and experience in key Company Key Therapeutic areas.
  • Strong written and verbal communication skills. Able to present with influence to Sr Management and Quality Leadership.
  • Strong and respectful negotiator and influencer. Demonstrated proficiency in conflict prevention and resolution.
  • Able to manage multiple complex projects, and demanding timelines
  • ASQ Certified Quality Auditor (CQA), ASQ Certified Manager of Quality/Organizational Excellence, or SQA Registered Quality Assurance Professional - GCP certification preferred, but not required.
  • Manual dexterity required to operate office equipment (i.e. computers, phones, etc.).
  • Carrying, handling and reaching for objects.
  • Ability to sit or stand for long periods of time while traveling.
  • Willingness to travel to various meetings and/or audits, including overnight trips. Some international travel may be required.
  • Requires approximately 30% travel.
skills: Quality Assurance
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

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