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AllucentAL

Site Contract Specialist (Contractor)

Allucent is a global clinical research organization (CRO) dedicated to helping small and mid-sized biotech companies bring new therapies to light by providing comprehensive drug development solutions, including consulting, clinical operations, biometrics, and clinical pharmacology.

Allucent

Employee count: 1001-5000

United States only

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Looking to expand your experience in site contracts and budget negotiations? Join a team where your work directly supports bringing life-changing therapies to patients worldwide.

We are looking for a talented Site Contract Specialist (Contractor) to partner with our A-team for a 4-month contract. As a Site Contract Specialist at Allucent, you will lead site-level contract and budget negotiations, partnering with global teams to move clinical trials forward efficiently.

At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.

The role:

  • In this role, you’ll be at the center of clinical trial start-up, working closely with sites and internal teams to negotiate contracts, manage budgets, and keep studies moving forward.
  • Take ownership of site contract and budget negotiations from draft through execution
  • Partner with global teams to keep timelines on track and sites activation-ready
  • Communicate with sites and stakeholders to resolve issues and move agreements forward
  • Identify risks and confidently recommend solutions or escalate when needed
  • Stay current on local regulations and requirements that impact contracts
  • This is a great opportunity if you enjoy problem-solving, collaboration, and working in a fast-paced, detail-driven environment.

Main responsibilities

  • Prepare, review, and negotiate clinical trial agreements (CTAs), budgets, and site contracts
  • Manage communication with sites and internal teams on contract status and timelines
  • Identify and escalate legal, financial, or operational risks
  • Track and maintain accurate data in CTMS and other systems
  • Support contract finalization, signatures, and documentation
  • Contribute to process improvements and quality initiatives

Requirements

About you / Who we’re looking for

  • You’re someone who enjoys owning your work, staying organized, and collaborating across teams to get things done.
  • Minimum 2 years’ experience in contract negotiations in clinical research or drug development area
  • Understanding of the clinical trial process and site start-up activities
  • Strong communication skills and confidence working with multiple stakeholders
  • Attention to detail with the ability to manage multiple priorities
  • Comfort working in a fast-paced, evolving environment
  • A degree in law, paralegal studies, or a related field (or equivalent combination of education, training and experience)

Why Join Allucent?

  • Exposure across multiple therapeutic areas
  • Flexible hybrid or remote work environment (based on location)
  • A collaborative, team-oriented culture
  • Ability to roll up your sleeves and apply your unique skill set, expertise, and knowledge to build partnerships with our clients in their pursuit to develop new, life-improving treatments.

Apply today and help shape our mission to bring new therapies to light!

About the job

Apply before

Posted on

Job type

Contractor

Experience level

Education

Bachelor degree

Experience

2 years minimum

Experience accepted in place of education

Location requirements

Hiring timezones

United States +/- 0 hours

About Allucent

Learn more about Allucent and their company culture.

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At Allucent, we are at the forefront of pioneering advancements in biopharmaceutical development, empowering small and mid-sized biotech companies to bring groundbreaking therapies to light. Our innovative approach integrates over 30 years of deep regulatory, therapeutic, and operational expertise to navigate the intricate landscape of clinical research and drug approval. Through cutting-edge solutions and a forward-thinking mindset, Allucent is revolutionizing how novel treatments reach patients globally. We leverage advanced data analytics, state-of-the-art clinical trial technologies, and adaptive study designs to accelerate development timelines and enhance the probability of success for complex therapeutic modalities, including oncology, rare diseases, cell and gene therapies, and infectious diseases.

Our commitment to innovation is exemplified by our strategic adoption of technologies like Artificial Intelligence for content development and data analysis, alongside sophisticated eClinical solutions such as Medidata Rave for optimized data capture and management. Allucent champions a patient-centric methodology, incorporating decentralized clinical trial (DCT) capabilities and real-world data to broaden patient access and improve the diversity and robustness of clinical evidence. By fostering a culture of continuous improvement and collaborative partnership, we provide our clients with the strategic insights and operational excellence required to overcome the unique challenges they face. Our global reach, spanning over 70 countries, combined with our dedicated 'A-Team' of seasoned experts, ensures that every project benefits from tailored strategies and meticulous execution, ultimately transforming scientific discoveries into life-changing medicines.

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Allucent

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