Senior Clinical Research Associate at IQVIA. - Turkey

Auckland, Auckland, New Zealand -

Full Time

Start Date

Immediate

Expiry Date

08 Feb, 26

Salary

0.0

Posted On

10 Nov, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

On-Site Monitoring, Oncology Trials, Haematology, GCP Knowledge, ICH Guidelines, Microsoft Office, Communication Skills, Organizational Skills, Problem-Solving, Time Management, Financial Management, Team Collaboration, Training, Site Management, Regulatory Submissions, Data Query Resolution

Industry

Hospitals and Health Care

Description

Currently seeking Senior Clinical Research Associate for our FSP team in New Zealand. Step into a dynamic role where you’ll drive innovation and excellence in clinical research. As a key player in our team, you’ll ensure that study sites are not just compliant but thriving, contributing to groundbreaking advancements in healthcare. Ideally Christchurch based and Oncology and Haematology monitoring experience is essential for this role. When you join IQVIA New Zealand as a CRA, you’ll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers. With access to world-class training and mentoring, you’ll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas. You must have a minimum of 4 years Independent on-site monitoring experience to be considered for this role. We regret to inform you that we can not consider sponsorship for this role at this stage so only candidates with full work rights will be contacted. You will be asked to complete a short video screening as part of the interview process. Essential Functions: Engage in Site Visits: From selection to close-out, your visits will be pivotal in ensuring the success of our studies. Recruitment Strategies: Develop and implement innovative plans to recruit study subjects, making a tangible impact on project outcomes Empower Sites with Knowledge: Provide essential training and maintain robust communication channels to keep sites aligned and motivated. Champion Quality and Integrity: Evaluate and enhance site practices, ensuring adherence to protocols and regulations. Drive Study Progress: Monitor every aspect of the study, from regulatory submissions to data query resolutions, ensuring seamless execution. Master Documentation: Keep meticulous records and ensure all site documents are perfectly maintained. Collaborate and Innovate: Work closely with a passionate team to support project execution and drive success. Manage Finances with Precision: Oversee site financials and ensure timely invoice retrieval. Qualifications: Educational Excellence: Bachelor’s degree in a scientific or healthcare discipline preferred. Experience Matters: At least 4 years of on-site monitoring experience, with preference for oncology trials and haematology. Regulatory Savvy: Strong knowledge of GCP and ICH guidelines. Tech-Savvy: Proficiency in Microsoft Office and relevant technology. Communication Pro: Excellent written and verbal skills. Organized and Analytical: Strong organizational and problem-solving abilities. Time and Financial Management: Effective in managing time and finances. Team Player: Ability to build and maintain strong relationships with coworkers, managers, and clients. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

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Responsibilities

The Senior Clinical Research Associate will engage in site visits to ensure the success of studies and develop innovative recruitment strategies for study subjects. They will also monitor study progress, maintain documentation, and collaborate with the team to drive project execution.