# Senior Clinical Research Associate

**Company**: Fortrea
**Location**: Sydney
**Experience**: senior
**Job type**: full-time
**Category**: Research
**Industry**: Healthcare

**Apply**: https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Sydney/Senior-Clinical-Research-Associate-I-II---FSP---Sydney-or-Melbourne_266710?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/job/senior-clinical-research-associate-ada2ef37-0f3/

## Description

Shape the Future of Clinical Research with Fortrea

As a Senior Clinical Research Associate, you will play a pivotal role in ensuring the success of clinical trials by managing and monitoring study sites. You'll work closely with investigators and sponsors to uphold regulatory standards and deliver high-quality data that advances medical breakthroughs.

**Key Responsibilities**

- Monitor and manage clinical study sites, including initiation, routine visits, and closeout activities.

- Ensure patient safety and compliance with informed consent and protocol requirements.

- Review source documents and verify data integrity on Case Report Forms (CRFs).

- Prepare accurate and timely monitoring reports and maintain study files.

- Serve as lead monitor for assigned protocols and assist in developing monitoring plans.

- Coordinate with vendors and internal teams to meet project timelines and objectives.

- Support feasibility assessments, budget negotiations, and regulatory submissions.

- Mentor and train junior team members through co-monitoring and guidance.

- Travel extensively (60–80%) to support site activities and maintain audit readiness.

**Qualifications**

- Bachelor's degree in life sciences or related field, or equivalent clinical research experience.

- Typically a minimum 3 years of clinical monitoring experience in pharmaceutical or CRO settings.

- Strong knowledge of regulatory requirements and drug development processes.

- Advanced site monitoring and management skills.

- Excellent communication, organisational, and problem-solving abilities.

- Proficiency in relevant computer applications and systems.

- Valid driver's license and ability to travel extensively.

**Why Join Fortrea**

- Contribute to groundbreaking research that improves lives worldwide.

- Access robust training, mentorship, and advancement opportunities.

- Thrive in a collaborative, inclusive environment that values work-life balance.

- Be part of a forward-thinking organisation shaping the future of clinical trials.

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## Skills

### Required
- life sciences
- clinical research
- regulatory requirements
- drug development processes
- site monitoring
- management skills
- communication skills
- organisational skills
- problem-solving skills
- computer applications

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Source: [Apply at fortrea.wd1.myworkdayjobs.com](https://fortrea.wd1.myworkdayjobs.com/en-US/Fortrea/job/Sydney/Senior-Clinical-Research-Associate-I-II---FSP---Sydney-or-Melbourne_266710?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)