Associate Procurement Specialist - OptymEdge

JOB_DESCRIPTION.SHARE.HTML

CAROUSEL_PARAGRAPH

JOB_DESCRIPTION.SHARE.HTML

• Bengaluru, India
• Procurement
• No
• Regular Full-Time
• 2841
  
  

Emmes Global

mail_outline

Get future jobs matching this search

or

Overview

Job Description

Job Posting Title

India Remote/Ahmedabad/Bengaluru/New Delhi

Emmes Group: Building a better future for us all.

Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience.

We believe the work we do will have a direct impact on patients’ lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We’re looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us!

Primary Purpose

The Associate Procurement Specialist is responsible for managing the procurement of clinical materials, equipment, and supplies, ensuring timely delivery to study sites. The ideal candidate is proactive, precise, and able to navigate both domestic and international sourcing requirements critical to clinical trial success.

Responsibilities

• Receive, review, and process internal purchase requests for clinical trial materials, lab supplies, and equipment.
• Source and submit orders to approved vendors, ensuring compliance with regulatory and quality standards.
• Track shipments of clinical trial supplies, providing status updates to stakeholders.
• Coordinate international shipments, including customs documentation, regulatory compliance, and tracking.
• Verify receipt of materials, ensuring accuracy, quality, and adherence to study specifications.
• Maintain organized records of purchase orders, shipments, vendor communications, and regulatory documentation.
• Assist in resolving issues related to delayed shipments, discrepancies, or damaged clinical materials.
• Support the procurement team in optimizing processes for efficiency and compliance in a clinical trial environment.
  
  

Qualifications

• Bachelor’s degree in Life Sciences, Business, Supply Chain, or related field preferred (or equivalent experience).
• Strong organizational skills and meticulous attention to detail.
• Excellent written and verbal communication skills.
• Proficiency with Microsoft Office Suite (Excel, Word, Outlook)
• Ability to manage multiple requests simultaneously and meet strict timelines.
• Willingness to learn about international shipping and regulatory requirements for clinical trial materials.
• Previous experience or internships in clinical trials, healthcare, or supply chain is a plus.
• Highly detail-oriented and methodical.
• Proactive problem solver with strong follow-through.
• Able to manage multiple tasks simultaneously.
• Collaborative and adaptable to a fast-paced clinical environment.
  
  

CONNECT WITH US!

Follow us on Twitter - @EmmesCRO

Find us on LinkedIn - Emmes

---