.We are seeking a Senior Contracts and Budget Associate to join our team!This is a remote-based opportunity open for professionals based in one of the following countries: UK, Spain, Hungary, Poland, Romania, Serbia or Slovakia.At Precision for Medicine, we believe that the era of one-size-fits-all medication is giving way to a next generation of treatments, medicines that will be more effective because they are prescribed according to the unique biology of an individual patient.
Our mission is to help innovative biotech and pharmaceutical companies accelerate the development of these life-changing treatments.
Precision does this by developing assays that utilize biomarkers to help identify the right patient for the right drug.We handle every aspect of clinical trials from initial strategy and design to selecting sites and executing quality clinical trials.Position Summary:The Senior Contracts and Budget Associate, Site Contract Management, develops and negotiates European study budgets based on the requirements of a study protocol, as well as reviewing, drafting, negotiating and tracking a variety of legal agreements which include confidentiality agreements, master confidentiality agreements, clinical study agreements and amendment agreements.
The postholder works closely with the Clinical Operations study team and plays a key role in ensuring deliverables are in alignment with defined study timelines.Essential functions of the job include but are not limited to:Develop, negotiate global study budgets based on the requirements of a study protocol.Review, draft and negotiate a variety of agreements including confidentiality agreements, master confidentiality agreements, clinical study agreements and amendment agreements.Work with supervisor and various internal/external key stakeholders to resolve/escalate contractual issues.Ensure adherence to company policies, procedures and contracting standards.Update relevant study team members regarding the status of contract negotiations and execution.Coordinate execution of agreements.Support the maintenance of contract files and databases, including contract archiving.Recognize where processes can be improved and take corrective action.Other tasks, as assigned.Qualifications:Minimum Required: Bachelor's degree, or equivalent level of contract management experience preferably in a clinical research or similar industry setting.Other Required: 3 years of relevant experience drafting, reviewing and negotiating agreements related to clinical research i.E.
Non-Disclosure Agreements, Clinical Trial Agreements, etc.
as well as management, control and tracking of the contract process.Experience in contract research, life science, biotech or pharmaceutical industry is preferred.Experience interacting with European institutions.Knowledge of English.Preferred: Equivalent contract management experience in a clinical research or similar industry setting