Vendor Qualification Associate

ATR International; San Mateo (CA); On-site; USD 55,000 - 63,000; Full time

Benefits offered by this job

Medical, dental, and vision benefits

401(k) retirement plan with employer-m

Lunch and transit benefits

Job summary

ATR International, Foster City, CA, is seeking a Vendor Qualification Associate to ensure data quality and service levels across vendors supporting the global R&D portfolio for Ph I-IV trials.

The role involves RFIs, privacy and security assessments, due diligence, and data analyses to deliver insights for strategic decisions. Strong communication and project management skills are essential to succeed in this position.

Qualifications

• BS or BA with 5 years of relevant experience.
• PMP certification or equivalent certification preferred.
• Executive presence, excellent communication skills, project management & critical thinking skills.
• Thorough knowledge of GCP, Good Pharmacovigilance, GLP, GDP and ICH E6 R2 compliance requirements.

Responsibilities

• Conduct RFIs and Data Privacy and Security IT Assessments.
• Perform Anti-Bribery and Anti-Corruption Due Diligence and Financial Health Assessments.
• Provide data analyses and benchmarking to inform strategies and continuous improvement.
• Deliver presentations and trainings.

Skills

Vendor capability assessments

Sourcing

Contracting

Procurement

Category management

Inspection readiness

Education

PMP certification or equivalent

BS or BA with 5 years of relevant experience

Job description

ATR International is hiring a Vendor Qualification Associate for a major client!

We are looking for a Vendor Qualification Associate, who will report to the Director of Vendor Outsourcing. The role will be responsible for ensuring high quality of data and services across all vendors supporting Company's global R&D portfolio - Ph I-IV clinical trials.

Location: Foster City, CA

Hourly Rate: $42.73

Details:

Responsible for ensuring high quality of data and services across all vendors supporting Company's global R&D portfolio - Ph I-IV clinical trials. Daily activities will include, but are not limited to, conducting Request for Information (RFI), Data Privacy and Security IT Assessments, Anti-Bribery and Anti-Corruption Due Diligence, Financial Health Assessments, Inspection Readiness Preparation Activities, Data Analyses and Benchmarking to Provide Data Informed Insights into Strategies and Continuous Improvement Initiatives, Presentations, and Trainings.

Requirements

Deep understanding of vendor capability assessments, sourcing, contracting, procurement, category management, and inspection readiness activities

• Understanding of various clinical trial activities such as clinical monitoring, data management, Real World Data/Evidence (RWD/RWE), biostatistics, medical writing, Ph 1 CRU, central lab, biomarker lab, bioanalytical lab, RTSM, eCOA, medical imaging, safety, e-informed consent, mobile HCP services, telemedicine and wearables/sensors
• BS or BA with 5 years of relevant experience
• PMP certification or equivalent certification preferred
• Executive presence, excellent communication skills, project management & critical thinking skills
• Demonstrates a thorough knowledge of Good Clinical Practice "GCP", Good Pharmacovigilance
• Practices "GVP", Good Laboratory Practice "GLP", Good Documentation Practice "GDP" and ICH E6 R2 compliance requirements
• Demonstrates a thorough understanding of current global and regional trends in compliance

Full-time employees (working an average of 30 hours or more) are eligible to select from different benefits packages. Packages may include medical, dental, and vision benefits, a 401(k) retirement savings plan with employer match (available after 1 year of employment), commuter benefits, employee discount and referral programs, and life and supplemental income insurance. Paid sick leave is provided in accordance with applicable state and local laws.

Compensation

Final offer amounts, within the base pay set forth above, are determined by factors including your relevant skills, education, and experience, as well as the benefits package you select.

Work Authorization

ATR International, Inc. cannot sponsor work visas (H-1B, F-1 STEM OPT with I-983, or similar). Candidates must have valid U.S. work authorization.

ATR International, Inc. is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.