General information

Organization

Orano Med is at the forefront of research in nuclear medicine and is developing new therapies against cancer. Based on its unique expertise in the production of lead-212 (Pb-212) and radiolabeling technologies, Orano Med is developing innovative radioligand therapies which consist of selectively destroying cancer cells while limiting the impact on surrounding healthy cells. With a solid portfolio of molecules in development capable of targeting various forms of cancer, and a reliable supply chain for Pb-212, Orano Med aims to become a leader in targeted alpha therapies, in particular for patients with currently unmet medical needs.

Find out more about Orano Med

Location

PLANO - Texas

Job details

Job description (internal)

Orano Med Theranostics

Are you passionate about ensuring the highest standards in pharmaceutical manufacturing? Do you thrive in a fast-paced, detail-oriented environment where your work directly impacts clinical trial success?

Join our Clinical Supply Chain team as Senior Manager, Clinical Supply Chain and play a vital role in safeguarding the integrity of raw materials and sterile drug products. Are you seeking your next challenge as Senior Manager, Clinical Supply Chain? If so, this is your chance to grow within a dynamic, mission-driven organization that’s transforming oncology from the inside out.

The Senior Manager, Clinical Supply supports day-to-day drug supply operations for Orano Med clinical trials, reporting to the Director of Clinical Supply. Key responsibilities include coordinating production schedules, tracking shipments, and resolving site-level supply issues to ensure timely drug delivery and dosing.

Key Responsibilities

Production and Delivery Coordination:

Assist the Director of Clinical Supply with coordinating radiopharmaceutical production schedules to align with site-specific dosing timelines
Manage logistics planning for dose deliveries from manufacturing sites to clinical sites, considering half-life constraints, time zones, and customs clearance.
Communicate regularly with manufacturing partners and courier vendors to confirm production status, pickup timing, and delivery confirmations

Order and Shipment Tracking:

Maintain and update internal tracking tools with real-time shipment status, from production through confirmed site receipt, including delivery confirmations and any delays
Proactively follow up with depots, clinical sites, courier vendors, and internal logistics stakeholders to ensure timely deliveries and address any in-transit issues or exceptions

Site and Vendor Communication Support:

Support the Director of Clinical Supply by assisting with site-facing logistics, including shipment tracking, drug availability, and receipt follow-up
Work closely with Clinical Operations, manufacturing, and vendor teams to help monitor schedule changes, resupply needs, and enrollment forecasts
Identify and document any shipment delays, temperature excursions, or discrepancies, and escalate to the Director for resolution

Cross-Functional Support:

Collaborate with cross-functional teams to align on enrollment projections, production scheduling, and logistics activities
Join recurring supply calls to keep internal teams informed of upcoming shipments and constraints
Support the Director in coordinating day-of dosing communications with manufacturers, couriers, and clinical sites

Skills and Qualifications (internal)

Education & Experience

Minimum Qualifications:

Bachelor’s degree in a relevant field (e.g., Supply Chain Management, Life Sciences, Pharmacy, or related discipline)
Minimum of 5 years of experience in clinical supply chain operations within the pharmaceutical or biotechnology industry
Experience coordinating day-to-day drug supply logistics in support of global or regional clinical trials
Prior experience supporting production and delivery timelines in partnership with third-party manufacturers and courier vendors

Required Skills & Competencies:

Strong operational understanding of clinical supply logistics, including production coordination, shipment tracking, and clinical site support
Familiarity with Good Manufacturing Practices (GMP), Good Distribution Practices (GDP), Good Clinical
Practice (GCP) and regulatory expectations for investigational products
Excellent organizational skills, with the ability to manage multiple time-sensitive priorities across sites, vendors, and manufacturing facilities
Strong communication and interpersonal skills, with the ability to work effectively across cross-functional teams and with external partners
Proactive problem-solving mindset with attention to detail and a focus on execution and issue escalation
Proficiency in Excel and supply tracking tools; working knowledge of IRT systems is preferred

Preferred Skills & Competencies:

Experience with radiopharmaceutical trials or time-sensitive drug products

Employment Classification

Regular/Permanent

Job

G - Project Management

Customizable block no. 2

Overtime status

Exempt

Relocation

Not specified

Job location

America / Caribbean / Canada, USA, Texas

Geolocation by area (Always put 'Yes')

Adress

Plano

Additional information

Telework/Home-office

Remote Options

Applicant criteria

Travel

Yes

Handled by

Primary manager

LeKeta DAVIS