At Illumina, you will lead global access strategies for our portfolio of diagnostic solutions pediatric and adult genetic disease as well as a portfolio of reproductive health solutions. Your work will help ensure that individuals and families around the world can benefit from early, accurate, and equitable access to life-changing genomic insights. This is a high-impact, strategic leadership role that requires deep expertise in diagnostic testing for rare and inherited conditions, and reproductive health.
Functions as a team member of the drug utilization review and medication management therapy programs within Clinical Pharmacy Services (CPS). Responsible for administering client-specific programs to provide clinical expertise in regards to prior authorization for member prescriptions and client member’s drug therapy. Participates in prospective and retrospective DUR activities including, but not limited to: handling live calls from physicians and pharmacists, reviewing appropriate drug therapy.
As a Medical Director, you will lead the clinical sub-team or support it and the global program team to build global clinical development plans and contributes to the development of asset level and therapeutic area strategies. You will be responsible for overseeing the clinical development strategy development and execution for 1 program, leading the clinical subteam, contributing to the development of regulatory strategy, and representing the clinical program at regulatory meetings
As a Sr. TAT (Targeted Alpha Therapeurics) Expert you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. The role involves site interactions, effective communication with site personnel, site setup, and training. Acts as targeted aplha therapeutic expert as a study team member for assigned project. Oversee operational radiotherapeutic aspects for global studies. Supports radiotherapeutic licenising activities and drug supply logistics
This is a remote position where the Clinical Pharmacist provides timely and accurate pharmaceutical care. Responsibilities include processing medication orders, providing drug information, monitoring for adverse reactions, and ensuring appropriate medication use. The role requires knowledge of pharmacy practice, state requirements, and regulatory guidelines.
The National Field Trainer supports the Rheumatology franchise organization in the design and delivery of training solutions to a field sales organization. The role requires a high level of performance coaching, strategy alignment/execution, and application of training fundamentals to enhance performance learning of participants. This is a remote role with up to 50% travel.
As a PK Scientist, you will perform protocol writing of Phase 1 clinical pharmacology studies, pharmacokinetic and/or pharmacodynamic analysis using non-compartmental methods, and reporting for clinical trials. Responsibilities include authoring protocols, coordinating development with study teams, reviewing dataset requirements, writing Clinical Pharmacology Analysis Plans, and drafting clinical pharmacology sections of Clinical Study Reports.
The Clinical Trial Manager (CTM) is a key member of Clinical Operations and will closely partner with the Associate Director, Clinical Program Management. Assist Clinical Program Manager with set-up of regional CRO and other vendors as required, including liaising with Global CRO to ensure site training and timely initiation. May serve as the key operational contact for Akero studies aiding in site selection, study implementation and ongoing coordination of study sites, either directly or via CROs.
Join our customer's team as a Pharmacist - AI Trainer and play a vital role in enhancing the accuracy and reliability of AI-powered medical platforms. Utilize your clinical expertise to review, train, and improve artificial intelligence systems, ensuring the delivery of high-quality, medically sound information for healthcare providers and patients.