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Clinical Contracts Associate - I
Career Insights for Pharmaceutical Manufacturing Process Engineer
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Scorecard
Based on California data
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What they do
A Pharmaceutical Manufacturing Process Engineer designs and maintains manufacturing equipment, facilities and processes for a pharmaceutical company. Maintains process controls for the specific sterile processing requirements of pharmaceutical manufacturing.
$121,138 / year median in California
+14% projected growth
Job Description
Clinical Contracts Associate - I at NexInfo Solutions, Inc. Clinical Contracts Associate - I at NexInfo Solutions, Inc. in Belmont, California Posted in 2 days ago.
Type:
full-time ????
Now Hiring:
Vendor Qualification Associate I ????
Location:
Foster City, CA - Hybrid/Onsite 3 days per week ????
Schedule:
Monday-Friday, 8:00 AM-5:00 PM ????
Type:
Contract | Potential for Extension ???? About the Role We are looking for a Vendor Qualification Associate I to support vendor qualification, oversight, and compliance activities across a global pharmaceutical/biopharmaceutical R D environment. ???? Key Responsibilities Conduct vendor Request for Information (RFI) and capability assessments Support Data Privacy & Security IT Assessments Perform Anti-Bribery & Anti-Corruption Due Diligence Support financial health assessments and vendor risk evaluations Assist with inspection readiness activities Perform data analysis, benchmarking, and continuous improvement initiatives Prepare presentations, reports, and training materials Collaborate with Clinical Operations, Quality & Compliance, Finance, Legal, and other cross-functional teams Partner with external vendors to support qualification and oversight activities ???? Required Qualifications Bachelor's degree in a relevant field 5+ years of relevant experience ; pharmaceutical/biopharmaceutical/healthcare experience strongly preferred Strong project management, analytical, and critical-thinking skills Excellent communication and stakeholder-management abilities Experience with vendor management, qualification, sourcing, procurement, contracting, or category management Strong knowledge of GCP, GVP, GLP, GDP, and
ICH E6 R2
Ability to independently manage multiple priorities PMP or equivalent certification preferred Current or former Project Managers from the Pharmaceutical or Healthcare industry are encouraged to apply ???? Preferred Background Candidates with experience supporting clinical trial vendors and activities such as Clinical Operations, Data Management, Biostatistics, Medical Writing, Central Labs, Biomarker/Bioanalytical Labs, RTSM, eCOA, Medical Imaging, Safety, eConsent, Telemedicine, or Wearables will be highly relevant. Apply now or send your updated resume to sudheer.batha@nexinfo.com