•Do you want to join a team that is developing technologies that will shape the future of drug discovery?
•Would you like an environment where you could make a major impact on a critically important industry?
•Would you like the opportunity to do things differently instead of just following tradition?
We are seeking the right person to join the Verseon team in our clinical development efforts. This is an opportunity to help build a world-class clinical organization from the ground up that sets the standard for efficiency and results. You will have a range of responsibilities, from helping evaluate clinical trial providers to being a point of contact for domestic and international regulatory agencies. The right person will bring new ideas to improve on traditional clinical trials processes and methods and is not afraid to question convention.
•Designing and implementing clinical research projects; building relationships with clinical advisory board members; maintaining contact with regulatory authorities; and preparation of regulatory briefing documents.
•Developing protocols, study-related documents, study manuals, and budgets.
•Negotiating site contracts and visiting sites to ensure progress.
•Reviewing clinical data and assisting in the preparation of interim study analyses, annual reports, and clinical study reports.
•Assisting in all aspects of IND and NDA submissions (and/or country-specific equivalents).
•PhD. in relevant scientific discipline and/or MD with at least five years of research experience.
•5+ years of industry experience in clinical trials
•Knowledge of GCP, ICH, FDA and EMA regulations
•Strong organizational skills, an attention to detail, and ability to multi-task effectively
•Strong written and verbal communication and interpersonal skills