We are Growing !
Let us support your career journey the Biorasi way.
Innovative, Collaborative, Dynamic and Evolving.
Capitalizing on your strengths while encouraging work-life balance.
Biorasi is an award-winning, customer-focused, full-service clinical research organization.
Biorasi is looking for top performers who are as passionate about clinical research as we are – clinical trial veterans and industry newcomers who will thrive in our fast-paced environment and help us drive new therapies to patients.
Here is your chance to become a vital part of a growing global company in the expanding clinical research industry.
Your role: Lead development, implementation, and maintenance of GCP Quality Systems and SOPs Train and mentor staff on global GCP regulations and guidance.
Provide QA oversight and auditing of eTMFs Lead and/or oversee consultant mediated audits; develop, recommend, and follow up on corrective actions Lead preparations for Clinical Operations (corporate and third-party) inspection-readiness Lead and manage GCP Inspections on behalf of Biorasi and Biorasi clients.
Serve as an SME for areas of responsibility during regulatory inspections, and directly manage inspection Ready -Room activities.
In partnership with the Clinical Operations, Regulatory, and Pharmacovigilance teams, design and implement a risk-based clinical Quality Assurance management system Identify QA and compliance related issues and implement solutions to ensure timelines are maintained Establish metrics and report the state of GCP Quality and compliance of clinical trials to senior management Ensure Clinical Operations activities are compliant with cGCP, cGLP, FDA, ICH, EMA regulations and guidelines and industry standards Provide consultation in interpretation of regulations/guidelines, as they apply to GCP practice, awareness of regional regulatory requirement, and phase of study and Keep abreast of industry developments – forthcoming regulations, guidance, best practices, etc.
Ensures that Biorasi quality systems, processes, and procedures are compliant with applicable regulations and ICH guidelines.
Ensures that Biorasi standard operating procedures (SOPs) are compliant with applicable regulations and guidelines.
Oversees the planning and conduct of internal, investigator, and vendor Quality Assurance audits.
Manages the administration of Quality Assurance files and the control of central files.
Your Profile: Degree in biomedical sciences, related scientific discipline.
10+ years in drug development or clinical research within the pharmaceutical industry or CRO with at least three years in quality assurance, quality management, or clinical safety related area of responsibility.
Strong planning, leadership, negotiation, communication, and presentation skills.
Experienced with auditing clinical vendors and investigator sites.
Practical knowledge of GCP or GMP, and FDA regulatory structure.
Proficient with Microsoft Office tools.
If you have the experience required and want to join an energetic, creative, and collaborative team, please apply directly to our website at https://biorasi.com or email us at ****** .
We strive to provide our employees and their families with benefits that are thoughtfully designed to enhance your health and well-being.
Our employees enjoy half-day Fridays, paid time off, paid holidays, extensive country specific benefits, employee bonus programs, career growth, training and development.
Biorasi is committed to creating a diverse environment and is proud to be an equal opportunity employer.
All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, or veteran status.
Biorasi is also committed to compliance with all fair employment practices regarding citizenship and immigration status.
