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JUPITER RESEARCH SERVICES INC

Manager - Comparator Sourcing (Clinical Trials) USA, EU and APAC Markets

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Job Description

Company Description

Jupiter Research Services has been a valued service partner for over 15 years, supporting Sponsors and CRO companies with challenging clinical trial requirements, including Comparator Sourcing, Storage & Distribution, Logistics & Supply Chain Management, and Clinical Consulting. Committed to delivering quality services and timely responses, Jupiter Research Services is recognized for providing on-time, cost-effective solutions.

Role Description

This is a full-time, on-site role for a Manager - Comparator Sourcing (Clinical Trials) USA, EU, and APAC Markets, located in Ahmedabad, Gujarat, India.

The Comparator Sourcing Manager will be responsible for end-to-end management of global comparator procurement for clinical trials, ensuring cost-effective, compliant, and timely supply. The role will also oversee ERP systems management, vendor negotiations, sales and revenue tracking, and quality compliance, while collaborating cross-functionally to meet client and project requirements.

Key Responsibilities

Comparator Sourcing & Procurement

  • Identify, qualify, and manage global suppliers for comparator drugs across multiple geographies.
  • Negotiate pricing, lead times, and supply terms to optimize cost and delivery performance.
  • Oversee tender processes, RFQs, and vendor contract execution.

ERP Systems & Data Management

  • Manage procurement, sales, and inventory workflows within ERP systems.
  • Maintain accurate product, supplier, and pricing master data.
  • Generate ERP-based reports for forecasting, performance monitoring, and decision-making.

Sales & Revenue Management

  • Support business development with market intelligence and competitive pricing strategies.
  • Monitor project profitability, revenue targets, and client relationship management.
  • Prepare quotations, proposals, and presentations in collaboration with commercial teams.

Quality & Regulatory Compliance

  • Ensure all sourcing activities comply with GDP, GMP, and regional regulations.
  • Coordinate vendor qualification, product release, and audit readiness.
  • Maintain documentation for regulatory inspections, CAPAs, and change controls.

Cross-Functional Collaboration

  • Work with logistics for temperature-controlled shipments.
  • Liaise with finance for budget tracking, invoicing, and payment.
  • Support project management to meet timelines and deliverables.

Key Performance Indicators (KPIs)
  • On-Time Delivery Rate % of comparator shipments delivered as per agreed timelines.
  • Cost Savings Achieved Reduction in procurement cost through strategic sourcing.
  • Vendor Compliance Rate % of approved suppliers meeting GDP/GMP standards.
  • ERP Data Accuracy Error rate in master data and transactional entries.
  • Revenue Growth Year-over-year growth in comparator sourcing revenue.
  • Client Retention Rate % of repeat clients for comparator services.
Qualifications & Experience
  • Bachelor's degree in Pharmacy, Life Sciences, Supply Chain, or related field (Master's preferred).
  • Minimum 5 years experience in pharmaceutical procurement, clinical trial supply, or related role.
  • Strong knowledge of GDP, GMP, and ICH GCP guidelines.
  • Hands-on experience with ERP systems (SAP, Oracle, NetSuite, or similar).
  • Proven negotiation skills with global suppliers.
  • Excellent communication, analytical, and problem-solving abilities.
  • Ability to work in a fast-paced, deadline-driven environment.
Why Join Us
  • Opportunity to work on global clinical trial projects.
  • Collaborative and growth-oriented work environment.
  • Competitive compensation and benefits package.

Qualifications

  • Experience in Comparator Sourcing and Logistics & Supply Chain Management
  • Clinical Trials related experience preferred
  • Background in Pharmaceutical Procurement & Sales, Storage & Distribution and Clinical Consulting
  • Strong project management and leadership skills
  • Excellent communication and interpersonal skills
  • Ability to work effectively in a team and manage multiple projects simultaneously
  • Familiarity with regulatory requirements in clinical trials
  • Bachelor's degree in Life Sciences, Pharmacy, Business, or a related field
  • Experience in the pharmaceutical or clinical research industry is a plus

More Info

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Job ID: 137603847