# Contract Analyst II

**Company**: ICON Strategic Solutions
**Location**: Reading
**Work arrangement**: remote
**Experience**: mid
**Job type**: full-time
**Category**: Consulting
**Industry**: Healthcare

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/UK-Reading/Clinical-Site-Contracts-Specialist_JR163162?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_e91abc98-67d

## Description

As a Contract Analyst II at ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise.

You will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

**Responsibilities**

- Review and analyse contracts, agreements, and legal documents related to clinical trial activities and vendor relationships.

- Negotiate contract terms and conditions with clients, vendors, and other stakeholders to ensure compliance with regulatory requirements and company policies.

- Prepare, negotiate, and finalise clinical trial agreements and ancillary agreements for company-sponsored and/or investigator-initiated studies.

- Work with global teams to review and analyse contractual terms and conditions, assessing legal and budget risks.

- Analyse investigator fees in relation to fair market value pricing and ensure alignment with regional standards and J&J pricing guidelines.

- Provide support for negotiations in confidentiality agreements, informed consent forms, and other ancillary contract documents.

- Participate in discussions related to the development of site/investigator budgets aligned with fair market value.

- Manage the contract amendment lifecycle.

**Your Profile**

- Bachelor's degree in business, life sciences, communications, or a related discipline.

- Minimum of 2 years of experience in contract administration, contract management, or a related field, in the pharmaceutical or clinical research industry.

- Strong understanding of contract law, legal terminology, and regulatory requirements related to clinical trials and vendor agreements.

- Excellent analytical and problem-solving skills, with the ability to evaluate complex contractual issues and propose effective solutions.

- Strong attention to detail and organisational skills, with the ability to manage multiple tasks and prioritise work effectively in a fast-paced environment.

**Rewards & Benefits**

- Competitive base salary and performance-related incentives.

- Health and wellbeing programmes, including medical, dental, and vision coverage where applicable.

- Retirement and pension plans.

- Life assurance and disability coverage.

- Employee assistance programmes and wellbeing resources.

- Learning and development opportunities through structured training and career pathways.

## Skills

### Required
- contract management
- contract law
- regulatory requirements
- analytical skills
- problem-solving skills

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Source: [Apply at icon.wd3.myworkdayjobs.com](https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/UK-Reading/Clinical-Site-Contracts-Specialist_JR163162?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)