Senior Clinical Research Associate for a Sponsor

Summary about this job

Detail information about job Senior Clinical Research Associate for a Sponsor. Terms and conditions vacancy

About the business

My client is a big CRO committed to providing high quality, structured and a professional approach to all phases of development to their clients.

They value your personal development so they offer a clear career progression path, offers an internal training program with a variety of opportunities and you will be joining a close-knit team.

The company has an excellent work environment with dedicated mentoring, promotions and other benefits. A unique opportunity to experience a range of different projects and at different stages to broaden your experience.

Job Tasks and Responsibilities

• Make sure the reported trail data is accurate, complete and verifiable from source document
• Supporting the development of a subject recruitment plan
• Establishing regular lines of communication plus administering protocol and related study training to assigned sites
• Preforming site selection visits to ensure sites have adequate resources to conduct studies
• Evaluating the quality and integrity of sits and escalating quality issues as appropriate
• Managing progress by tracking regulatory submissions, recruitment and data query resolution 

Skills and experience

• At least 18 months' experience in independent monitoring (Oncology desirable) in Australia or New Zealand
• Degree in Clinical or Life Science related field (relevant experience in similar professions may also be considered
• Solid knowledge of GCP
• Excellent interpersonal and team skills
• A strong track record of preforming visits to site according to the Clinical Monitoring Plan
• Seeking someone highly collaborative and want to grow in what they do