Research Pharmacist

ICON plc • Lenexa, KS

5d • Onsite

About The Position

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

Requirements

• Bachelor’s degree or international equivalent
• 5 years of relevant experience
• Working knowledge of pharmaceutical formulations

Responsibilities

• Inspects and dispenses experimental drugs for clinical trial patients.
• Reviews and edits clinical protocols, batch records / preparation records and investigational medicinal product dossier (IMPD), if applicable, by generating, collecting and analyzing trial data.
• Oversees the manufacturing aspect of the Chemistry, Manufacturing and Control (CMC) projects when working in a good manufacturing practice (GMP) environment.
• Serves as a resource for investigational drug-related inquiries.
• Maintains drug accountability by compiling and documenting the accurate dosage for patients.
• Advises medical staff on investigational medicinal product (IMP) (e.g. use, type and route of administration).
• Plans and evaluates IMP programs and regimens by ensuring processes, data and samples are recorded and stored properly.
• Drafts manufacturing/compounding batch records.
• Manages facility parameters to ensure CMC projects are conducted in compliance with GMP, if applicable.
• Reads and reviews IMPDs or Investigational New Drug (IND).

Benefits

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level