P

Parexel

End-to-end clinical trials and regulatory consulting

SCA/Senior SCA/SCL

Contract ManagementConfirmed live in the last 24 hours
Full-timeShenyang, Liaoning, ChinaNo salary listedIn-person

About the Job

Requirements

  • Bachelor's degree in a related field, such as law, economics, business, or social sciences, or equivalent training or industry experience.
  • Strong negotiation, diplomacy, organizational, interpersonal, verbal, and written communication skills, with demonstrated experience handling multiple projects.
  • Strong problem-solving and analytical skills, including the ability to create or interpret legal language and budgets.
  • Ability to work successfully in a virtual team environment, align internal and external resources, and maintain professionalism under pressure.
  • Attention to detail; ability to comprehend contract language, independently identify problems and execute solutions, and act quickly toward desired objectives.
  • Polished presentation skills and a quality-driven approach to managed activities.
  • Fluent written and spoken English; additional languages are beneficial.
  • Solid working proficiency with Microsoft Office products, specifically Excel, Word, and PowerPoint.
  • SCA I is an entry-level role and does not require specific industry experience.

Responsibilities

  • Draft, review, and negotiate site agreements, including clinical study agreements, service agreements, team member agreements, and related letters, notices, and documents.
  • Provide context for comments received from sites based on local legal and business frameworks, common practices, and past negotiation experience to support further review and decision-making.
  • Apply and scrutinize site contracts and related document revisions against negotiation and budget parameters, as applicable.
  • Ensure final documents comply with applicable laws, regulations, and guidelines, including ICH-GCP.
  • Ensure the interests of both clients and Parexel are met.
  • Serve as the key communication liaison between site contract staff and internal and external customers; provide functional guidance, keep teams informed of contract statuses and pending issues, and prepare correspondence as needed.
  • Manage contract execution, including obtaining required signatures and ensuring timely execution by all parties.
  • Follow record maintenance and archival guidelines and ensure archived records are adequate and accurate.
  • Develop and maintain positive relationships with clinical trial sites.
  • Maintain a thorough understanding of the clinical trial protocol, budget, and timelines so contract terms align with trial goals and objectives.
  • Identify potential issues with contract terms and collaborate with internal stakeholders and clinical trial sites to find mutually acceptable solutions.
  • Stay current with relevant regulatory requirements, guidelines, and applicable laws in the respective country.
  • Verify that documents required for clinical site agreements, including powers of attorney, insurance certificates, indemnification letters, informed consent forms, referenced agreements, and other related documents, are aligned and in place.
  • Track and report site-contracting activity status to the Site Contract Lead, internal stakeholders, and study teams.
  • Perform self-checks and review contracts for completeness and accuracy to ensure first-time quality.
  • Ensure changes are appropriately made, approved, and documented.
  • Work within forecasted country and site contracting timelines, track compliance and milestone progress in the agreed contract-tracking system in real time.
  • Identify potential contract or process operational risks and proactively work with the Site Contract Lead to provide solutions.
  • Review and comply with standard operating procedures and other applicable guidance in a timely manner, keep training records updated, and ensure timesheet compliance.
  • Identify and implement process improvements to increase efficiency and quality in site contracting.
  • Provide guidance and support to study teams and project management on site-contracting matters in the respective country.
  • Participate in cross-functional communication to identify process improvements and contribute to site-contracting strategy development.

Desired Qualifications

  • Command of additional languages.

About the Company

Parexel

End-to-end clinical trials and regulatory consulting

Parexel provides end-to-end clinical development services for pharmaceutical, biotechnology, and medical device clients from Phase I to Phase IV. Its offerings include clinical trial management, regulatory consulting, and biostatistical analysis to support the design, execution, and analysis of clinical studies. The company operates as a CRO, partnering with sponsors to manage trials, ensure regulatory compliance, and generate robust data for drug development. What sets Parexel apart is its breadth of services across the trial lifecycle, emphasis on quality and reliability, and industry recognition, along with a focus on patient-centric approaches and leadership in gender partnership. The company’s goal is to help clients bring new therapies to market efficiently and safely by delivering high-quality, compliant trial outcomes and data that support regulatory submissions.

Company size
10,001+
Company stage
Acquired
Total funding
$8.5B
Headquarters
Durham, NC
Founded
1982

Recently Posted Jobs

Explore more opportunities at Parexel

See more jobs