Jobs in All Categories (14) Operations & General Management (1) Science & Education (13)
Identify and validate pharmacodynamic biomarkers to support preclinical and clinical development.
Ability to manage the technical needs of projects, and to concisely communicate results and recommendations in a project team setting is a must.
The successful candidate will independently manage the technical and strategic needs of projects, interface with scientific staff within and outside, including academic collaborations, external consultants and CROs.
Ability to independently manage the technical and strategic needs of multiple simultaneously progressing projects in a project team setting is a must.
The QA director will be responsible for oversight and implementation of quality systems in line with regulations.
Experience collaborating with external GMP CMOs to manage tech transfer activities, design of experiments, and review of analytical study protocols & reports.
Responsible for tracking project status and aligning FORMA organizational goals with available project resources.
Develop and manage comprehensive study timelines and metrics and ensures completion of study deliverables.
Set the overall vision and direction for the project and serve as visible project champion and focal point for critical project information.
Responsible for working with teams to identify appropriate ADME/PK issues and strategies to support candidate selection and clinical evaluation.
Write statistical sections of protocols and manuscripts for Phase I-IV clinical trials in oncology and non-oncology.
Provide and coordinate day to day managing issue resolution with vendors.
Provide and coordinate day to day support of research applications including desktop support, training, ongoing account administration, and managing issue resolution with vendors.
Analyze genetics drop-out screens data using bioinformatics tools.