Associate Director, R&D IT at Perspective Therapeutics

Coralville, Iowa, United States -

Full Time

Start Date

Immediate

Expiry Date

17 May, 26

Salary

0.0

Posted On

16 Feb, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Strategic Leadership, Technology Roadmaps, System Lifecycle Management, Computer System Validation, GxP Compliance, 21 CFR Part 11, Data Integrity, Change Control, IT Service Delivery, Facility Expansion, Manufacturing Enablement, Cross-functional Initiatives, Vendor Management, Root-Cause Analysis, Cybersecurity, Inspection Readiness

Industry

Pharmaceutical Manufacturing

Description

Objective The objective of the Associate Director, R&D IT role is to provide strategic, hands-on technology leadership across the full R&D lifecycle—enabling Clinical Development, Clinical Operations, Preclinical/Discovery, Regulatory Affairs, Quality (QA/QC), CMC, Operations, and Supply Chain with modern, scalable, compliant digital solutions. The role also ensures Phase 3 readiness, including the digital, data, and system capabilities needed for late‑stage clinical execution and regulatory scrutiny. The role exists to ensure Perspective Therapeutics' R&D and Operations teams have the right applications, data foundations, integrations, and operational capabilities to accelerate asset development, improve data quality, strengthen compliance, and support efficient radiopharmaceutical development and manufacturing. This includes supporting computer system validation (CSV), inspection readiness, and enabling digital infrastructure for new manufacturing plant buildouts, ensuring systems and processes meet regulatory, quality, and operational requirements from construction through commercialization. **** This is an onsite position in Coralville, Iowa and will only consider candidates eligible to work in the US without sponsorship **** Essential Functions Strategic Leadership & Alignment: Provide strategic IT leadership across R&D, Clinical, Regulatory, Quality, CMC, Operations, and Supply Chain, ensuring technology initiatives align with scientific, operational, and compliance priorities. Define and drive technology roadmaps that support Phase 3 readiness, operational scale-up, and long‑term digital maturity. Systems Ownership, Lifecycle Management & Validation: Oversee implementation, optimization, and lifecycle management of scientific, clinical, regulatory, quality, and manufacturing systems. Lead system validation activities, including authoring and reviewing Computer System Validation (CSV) deliverables in alignment with GxP, 21 CFR Part 11, data integrity, and internal SOPs and IT Policies. Maintain accountability for system administration, configuration management, change control, and ongoing maintenance across R&D, Clinical, Quality, and Operations applications. Operational Excellence & IT Service Delivery: Ensure reliable day‑to‑day IT Lab operations in partnership with managed service providers, maintaining system uptime, cybersecurity standards, and white‑glove end‑user support. Drive governance of IT procedures, SOPs, validation documentation, and operational controls to uphold regulatory and site‑readiness requirements. Facility Expansion, Manufacturing Enablement & Infrastructure Readiness: Support new facility buildouts by enabling digital infrastructure planning, system selection, commissioning, qualification, validation, and readiness for clinical and commercial manufacturing. Lead cross‑functional initiatives supporting clinical trial execution, regulatory submissions, inspection readiness, and manufacturing scale-up. Education/Experience Bachelor’s degree in Information Technology, Computer Science, Engineering, or a related field; advanced degree preferred. 7+ years supporting Clinical, Regulatory, Quality, CMC, Operations, or R&D IT systems in biotech/pharma. Experience with validated systems, Change Control, Computer System Validation, and regulated system governance. Hands-on experience with scientific, clinical, quality, regulatory, or manufacturing applications. Demonstrated experience leading cross‑functional initiatives and partnering with scientific, clinical, regulatory, and operations leaders. Experience leading or mentoring technical staff, vendors, or cross‑functional project teams. Experience managing IT vendors, contracts, and budgeted initiatives. Preferred Qualifications Experience providing remote IT support across distributed teams. Experience supporting radiopharmaceutical or highly regulated manufacturing environments. Familiarity with isotope development, analytical chemistry, and QC/QA laboratory workflows. Experience supporting manufacturing site buildouts, commissioning, qualification, and validation. Understanding of regulatory frameworks such as GxP, 21 CFR Part 11, data integrity, FDA, and nuclear regulatory requirements. Familiarity with LIMS, ELN, CTMS, eTMF, QMS, RIMS, and other scientific/clinical systems. Experience working with outsourced IT providers or hybrid internal/external support models. Understanding of compliance and cybersecurity frameworks relevant to regulated environments (e.g., GxP, SOX, HIPAA, GDPR). Knowledge / Skill / Abilities Excellent written, verbal, and presentation skills; able to communicate effectively across scientific, regulatory, quality, and operational functions. Strong analytical and problem‑solving abilities, including root‑cause analysis in regulated environments. Ability to manage competing priorities, operate both strategically and tactically, and work independently or collaboratively. Strong organizational skills with attention to detail and documentation rigor. Proven ability to build effective cross‑functional relationships and operate as a trusted advisor. Work Environment The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. This role is based out of Perspective’s Coralville, Iowa offices and labs. Travel up to 30% to meet the ongoing needs of the business might be required. Must be willing to work in a facility producing radioactive materials and requiring all employees to participate in safety programs designed to minimize potential and/or actual exposure levels Mechanical aptitude required; manual dexterity for manipulating small items; ability to lift up to 50 lbs. and to handle frequent crawling, stooping, crouching, and kneeling Must be willing to wear a variety of personal protective equipment Willingness to complete safety training within allotted timeframes, and work in a team-based environment This job description reflects key responsibilities and expectations and may evolve as business needs change. Perspective Therapeutics provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training. For information on Perspective Therapeutics, visit our website at: www.perspectivetherapeutics.com.

How To Apply:

Incase you would like to apply to this job directly from the source, please click here

Responsibilities

This role provides strategic, hands-on technology leadership across the full R&D lifecycle, ensuring teams have the necessary digital solutions, data foundations, and integrations to accelerate asset development and improve compliance. Key functions include overseeing system validation, managing IT operations, and enabling digital infrastructure for new manufacturing plant buildouts from construction through commercialization.