Senior Contract Analyst at Jobgether

, , Australia -

Full Time

Start Date

Immediate

Expiry Date

14 Sep, 26

Salary

0.0

Posted On

16 Jun, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Contract Negotiation, Contract Administration, Clinical Research Contracts, Risk Analysis, Stakeholder Management, Regulatory Compliance, Legal Interpretation, Project Support, Time Management, Analytical Skills, Contract Drafting, Cross-functional Collaboration

Industry

Internet Marketplace Platforms

Description

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Senior Contract Analyst based in Australia. This is a key role within a global clinical research environment, focused on managing, reviewing, and negotiating contractual agreements that support the delivery of innovative biotech and pharmaceutical studies. You will act as a critical link between internal study teams and investigative sites, ensuring contracts are accurate, compliant, and aligned with regulatory and operational requirements. The role combines legal/contractual expertise with practical project support in a fast-paced, international setting. You will contribute directly to the efficiency and integrity of clinical trial execution, helping enable the development of new therapies. Working within a standardized global framework, you will collaborate closely with stakeholders across Australia and beyond. This position is ideal for a detail-oriented professional who thrives in structured yet dynamic environments where precision and accountability are essential. \n Accountabilities Review, draft, and negotiate clinical research contracts with investigative sites and internal stakeholders, ensuring compliance with applicable regulations, SOPs, and organizational policies. Analyze contractual terms and conditions to identify risks, inconsistencies, and improvement opportunities while ensuring clarity of obligations and deliverables. Provide expert guidance to study teams on contract interpretation, compliance requirements, and legal/operational implications. Maintain accurate contract records, tracking key milestones, deadlines, amendments, and execution status across assigned projects. Support the development and continuous improvement of contract management processes, templates, and best practices to enhance efficiency and risk mitigation. Collaborate with cross-functional teams to ensure smooth contract flow and timely execution within clinical trial timelines. Ensure alignment with global FSP standards and working practices while adapting to Australian regulatory and site-specific requirements. Requirements Bachelor’s degree in Business, Law, Legal Studies, or a related discipline; advanced qualifications in contract management are a plus. Proven experience in contract administration, negotiation, or contract management within the pharmaceutical, biotechnology, or clinical research (CRO/FSP) industry in Australia. Strong understanding of contract law principles, regulatory frameworks, and clinical research industry standards. Excellent analytical skills with the ability to interpret complex contractual language and identify risks and opportunities. High attention to detail with strong organizational and time management skills in a deadline-driven environment. Ability to manage multiple contracts and priorities simultaneously while maintaining accuracy and compliance. Strong communication and stakeholder management skills, with the ability to collaborate effectively across global and cross-functional teams. Benefits Competitive salary aligned with experience and market standards Home-based/remote working arrangement within Australia Flexible working environment supporting work-life balance Comprehensive health insurance options for you and your family Retirement and savings support programs Employee Assistance Programme providing 24/7 confidential support services Additional country-specific benefits such as wellness support, transport subsidies, or lifestyle allowances Opportunity to work in a global clinical research organization contributing to innovative biotech and pharmaceutical development \n How Jobgether works: We use an AI-powered matching process to ensure your application is reviewed quickly, objectively, and fairly against the role's core requirements. Our system identifies the top-fitting candidates, and this shortlist is then shared directly with the hiring company. The final decision and next steps (interviews, assessments) are managed by their internal team. We appreciate your interest and wish you the best! Why Apply Through Jobgether? Data Privacy Notice: By submitting your application, you acknowledge that Jobgether will process your personal data to evaluate your candidacy and share relevant information with the hiring employer. This processing is based on legitimate interest and pre-contractual measures under applicable data protection laws (including GDPR). You may exercise your rights (access, rectification, erasure, objection) at any time. #LI-CL1

Responsibilities

Review, draft, and negotiate clinical research contracts with investigative sites while ensuring compliance with regulations and SOPs. Provide expert guidance to study teams and maintain accurate contract records to support clinical trial execution.