Clinical Trials

2 weeks ago

Gautam Budh Nagar, India Ikris Pharma Network Pvt Ltd Full time

**Job Description - Clinical Trials & RLD Sourcing Executive**

**Job Title**: Clinical Trials & RLD Sourcing Executive
**Location**: Noida, Sector-62

**Job Type**: Full-time
**Experience**: 2-3 years (Experience)

**Job Summary**:
**Key Responsibilities:1. RLD & Clinical Trial Supply Sourcing**
- Identify and procure **Reference Listed Drugs (RLDs)** and comparator drugs for clinical trials.
- Collaborate with pharmaceutical manufacturers, distributors, and suppliers globally to ensure timely procurement.
- Evaluate and negotiate costs, lead times, and quality standards with vendors.
- Ensure compliance with regulatory guidelines for sourcing and import/export of RLDs.

**2. Regulatory & Compliance Management**
- Ensure that all procured RLDs comply with **FDA, EMA, CDSCO, and other regulatory authority standards**.
- Work closely with regulatory teams to maintain necessary documentation and certificates (CoA, CoPP, MSDS, Batch Release, etc.).
- Stay updated on **global regulations for clinical trial supplies, bioequivalence studies, and RLD procurement**.

**3. Vendor & Supplier Management**
- Develop strong relationships with international and domestic pharmaceutical companies for reliable sourcing.
- Evaluate supplier performance and ensure quality control standards.
- Handle contracts and agreements with vendors for long-term supply chain stability.

**4. Logistics & Supply Chain Coordination**
- Manage import/export logistics and handle necessary permits for the shipment of RLDs and clinical trial materials.
- Work with logistics partners to ensure timely and compliant delivery.
- Maintain accurate records of procurement, shipments, and inventory.

**5. Business Development & Market Research**
- Identify **new market opportunities** for RLD sourcing and clinical trial support services.
- Support business development efforts by identifying potential partnerships with CROs, pharma companies, and research organizations.
- Conduct market research on drug availability, pricing, and regulatory changes.

**Required Skills & Qualifications**:

- **Bachelor’s/Master’s degree in Pharmacy, Life Sciences, Biotechnology, Business Administration, or a related field.**:

- years of experience in **pharmaceutical sourcing, clinical trial supply management, or regulatory affairs**.
- Strong knowledge of **RLD procurement, bioequivalence studies, and clinical trial supply chains**.
- Familiarity with **global pharmaceutical regulations (FDA, EMA, CDSCO, MHRA, etc.)**.
- Excellent negotiation, communication, and vendor management skills.
- Ability to multitask and manage international supply chain operations efficiently.
- Proficiency in **MS Office, SAP, or other supply chain management software** (preferred).

**Why Join Us?**
- **Opportunity to work in a fast-growing sector** supporting clinical research and global drug development.
- **Exposure to international markets and regulatory frameworks.**:

- **Competitive salary and career growth opportunities.**:

- **Dynamic and collaborative work environment.**

**How to Apply**:
**Job Types**: Full-time, Permanent

Pay: From ₹10,000.00 per month

Schedule:

- Day shift
- Fixed shift

**Education**:

- Bachelor's (required)

Work Location: In person

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