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The Manager of Site Contract Management will oversee the Site Contracts team, ensuring contracts are delivered efficiently and align with study timelines. Responsibilities include participating in the development of processes and policies, managing contract metrics, collaborating with stakeholders, negotiating various agreements, and acting as a Subject Matter Expert in meetings.
Develop client-focused budgets and proposals for Phase I-IV clinical trials. Coordinate RFP responses and collaborate with global operational teams. Support Work Order and RFI deliverables as needed.
The Quality Assurance Specialist II ensures compliance with GxP quality systems in a laboratory setting. Responsibilities include managing quality events, conducting internal and supplier audits, maintaining quality metrics, supporting validation activities, and mentoring personnel on quality practices. This role participates in daily operations as a QA representative.
The Sr. Accountant will oversee daily operations related to the general ledger, banking, invoicing, and account reconciliations. Responsibilities include ensuring accurate financial reporting, managing payables and receivables, supporting financial closings, and enhancing workflow procedures. The position involves collaboration with finance teams and responding to inquiries from upper management.
Seeking a Senior Talent Acquisition Specialist to deliver full life cycle recruiting services in a CRO setting. Responsibilities include sourcing candidates, building talent communities, and collaborating with hiring managers. Required qualifications include a Bachelor's degree and 5+ years of recruiting experience in CRO roles.
The Data Engineer will implement and maintain data standards across laboratory services, focusing on data management, data processing, and quality control pipelines for biomarker data. Responsibilities include writing source code for data delivery, executing QC processes, collaborating with teams, and validating source code.
The Senior Statistical Programmer will lead SAS programming tasks for clinical studies, ensuring adherence to CDISC standards and regulations. Responsibilities include dataset generation, quality control, client interaction, and mentorship of junior programmers. The role requires strong programming skills, organizational abilities, and the capacity to support clinical trial data analyses.
The Manager Centralized Visit Report Reviewer leads and manages a team focused on ensuring the quality of clinical trial reports. The role involves mentoring, improving operational standards, providing strategic oversight, and ensuring compliance with regulatory requirements while fostering individual career development.
The Legal Counsel - Contracts provides legal support for client and vendor negotiations and handles various contractual matters. Responsibilities include drafting and reviewing legal agreements, offering counsel to business units, maintaining relationships, and ensuring contract compliance and execution. Additional duties include managing contract processes and staying updated on legal changes.
The Principal Quality Assurance Auditor oversees quality and compliance activities during clinical studies, serving as a subject matter expert, conducting and coordinating various audits, developing training, and ensuring adherence to regulations and company policies.
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