Senior Contracts and Budget Associate

Posted 16 Days Ago
Be an Early Applicant
Hiring Remotely in Budapest
Remote
Mid level
Biotech
The Role
The Senior Contracts and Budget Associate develops and negotiates study budgets and manages the drafting and negotiation of various legal agreements for clinical trials. They collaborate with clinical operations teams to align contractual deliverables with study timelines and maintain contract files and databases.
Summary Generated by Built In

We are seeking a Senior Contracts and Budget Associate to join our team! 

This is a remote based opportunity open for the 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:

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 playing 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.
  • Experience in contract research, life science, biotech or pharmaceutical industry.
  • Experience in direct negotiations with institutions based in Italy, UK and Spain.
  • Direct negotiations with institution based in France and Benelux countries will be a plus.

Skills:

Competencies

  • Possesses strong organizational/written communication skills and the ability to multi-task and prioritize in a fast-paced environment.
  • Executes time-sensitive matters while maintaining accuracy and attention to detail.
  • Exhibits high self-motivation and is able to work and plan with some supervision as well as in a global team environment.
  • Demonstrates a high degree of professionalism, as evidenced by punctuality, ability to deliver on commitments, an understanding of the service culture and positive interactions with customers and teammates, including good interpersonal skills.
  • Displays sound business judgment and a proactive, independent work style.
  • Is proficient in MS Office software programs and computer applications.
  • Handles sensitive issues with discretion.
  • Works well independently and cooperatively with others to achieve common goals in a virtual environment.
  • Develops, maintains, and strengthens relationships with others inside or outside of the organization who can provide information, assistance, and support

Precision for Medicine is revolutionizing the attack on cancer and we are passionate about helping you harness its power. We strike tumors on a molecular level using biomarkers to link specific mutations to specific treatments. We combine deep science with deep data from advanced technological platforms, then layer on specialized expertise in the design and execution of targeted, adaptive clinical trials. Ultimately, we deliver robust insights that inform real-time decisions and optimize the oncology development pathway.

#LI-NC1 #LI-Remote





Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.

Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law. © 2020 Precision Medicine Group, LLC

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [email protected].

It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.


The Company
HQ: Bethesda, MD
1,114 Employees
On-site Workplace

What We Do

Precision is the first global precision medicine clinical research services organization, purpose-built to improve the clinical research and development process for new therapeutics. Our novel approach integrates clinical operations excellence, with laboratory expertise, and advanced data sciences to inform every step. This maximizes our clients’ insight into patient biology, delivering more predictable trial outcomes and accelerating clinical development. We apply our expertise to trials at all stages—from early development through approval—with embedded experience in oncology and rare disease. With over 2000 dedicated professionals and 35 offices worldwide, we stand ready to help accelerate life-changing treatments anywhere around the globe.

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