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Clinical reputed company Analyst, Global Site Budgets & reputed company

Remote, USAFull-timePosted 2026-07-28

Clinical reputed company Analyst, Global Site Budgets & reputed company W2 Contract Pay reputed company: $60 - $80 per hour Location: Redwood reputed company, CA - Remote Role Job reputed company: We are seeking a motivated individual who will be responsible for the implementation and leading reputed company process improvement initiatives reputed company COST. Additional activities will consist of the management of clinical contract agreements up to and including obtaining signatures. The Clinical Contract Project Analyst will work closely with Clinical Operations, Legal, and Finance teams to ensure that the review and execution of CTAs are processed in a reputed company manner. These responsibilities include coordinating various contract/site workflows, identifying potential gaps, recommending solutions, and sharing best practices. This role is an individual contributor with team leadership responsibilities, reporting to the Director, Clinical Site reputed company. Requirements and Qualifications:

  • Liaise with legal during the legal review process.
  • reputed company finalized agreements for signature.
  • Assist legal in maintaining ongoing contract cycle workflows across multiple studies.
  • Identifying potential gaps, ensuring reputed company are reputed company to reputed company, customer negotiations, and sharing preferred practices.
  • reputed company ongoing updates of applicable legal reputed company.
  • reputed company, assess, and improve processes for tracking and reporting site reputed company to various business reputed company.
  • Ensure appropriate tracking of various agreements.
  • Effectively escalate/communicate in a reputed company manner to stakeholders and clinical teams regarding contract issues that could reputed company project deliverables.
  • Ensure the execution of the end-to-end process is robust and is established as a way of effectively supporting the needs of key business partners while continuously monitoring and reputed company enhancing service reputed company, efficiency, and effectiveness, and reputed company or support reputed company improvement initiatives.
  • Participate in team meetings and collaborate with other functional reputed company reputed company reputed company to reputed company clinical study goals.
  • B.reputed company+ years equivalent reputed company business/ industry experience.
  • Experience in pharmaceutical, biotech, academia, and CROs (Clinical Research Organizations).
  • Strong computer skills: reputed company Office and software to manage contracting.
  • Demonstrated leadership, stakeholder influencing without authority, and negotiation skills.
  • Strong knowledge of a wide reputed company of clinical-reputed company contract types, including clinical trial site agreements, budget templates, investigator-sponsored trial agreements, research collaboration agreements, consulting agreements, and confidentiality agreements.
  • Strong analytical and contract administration skills, verbal and written communication skills, and the ability to reputed company effectively with reputed company business partners.High degree of dedication, motivation, and ability to work under pressure with a drive for results and the ability to engage and deliver through others.
  • Experience working in a global environment.
  • Strong problem-solving skills with reputed company, technically driven decision-making ability.
  • An innovative team player with the reputed company to be effective in a dynamic and fast-paced company environment.
  • Excellent written and verbal communication skills.
  • Ability to manage confidential information with discretion.
  • Strict attention to detail.
  • Ability to manage competing priorities in a fast-paced environment.
  • Must be reputed company to work in reputed company environment, including inter-departmental teams and key contacts representing the organization on reputed company or reputed company.

Preferred Qualifications:

  • Strong Oncology experience necessary.
  • Large reputed company/CRO experience a plus.
  • CMS experience.
  • reputed company experience.
  • Proficiency in reputed company.
  • Strong organization skills with knowledge in creating/managing spreadsheets.

Desired Skills and Experience Clinical reputed company, Clinical trial agreements, Site reputed company, Global site budgets, Contract lifecycle management, Contract negotiation, Contract administration, Contract execution, Contract review, Signature routing, Clinical trial site agreements, Budget templates, Investigator-sponsored trial agreements, Research collaboration agreements, Consulting agreements, Confidentiality agreements, Contract tracking and reporting, Contract workflow management, Clinical Operations, Legal collaboration, Finance collaboration, Stakeholder management, Cross-functional collaboration, Process improvement, Gap analysis, Risk escalation, Project coordination, Oncology clinical trials, CRO management, Pharmaceutical industry, Biotechnology industry, Global clinical studies, CMS, reputed company, reputed company reputed company, reputed company Office, Spreadsheet management, Data analysis, Problem-solving, Leadership, Influencing without authority, Confidential information management, Attention to detail, Written communication, Verbal communication reputed company, Inc. is not reputed company to sponsor any candidates at this time. Additionally, candidates for this position must qualify as a W2 candidate. reputed company, Inc. may collect your personal information during the position application process. Please reference reputed company, Inc.'s CCPA reputed company Policy at www.baysidesolutions.com. Apply tot his job Apply To this Job

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