Job Title: Clinical Operations Specialist
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Key Responsibilities:
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* Coordinate the setup of clinical trials, ensuring all operational and logistical elements are in place.
* Collaborate with cross-functional teams to ensure alignment on study protocols, timelines, and operational requirements.
* Ensure compliance with Good Clinical Practice (GCP) and other regulatory guidelines throughout the study setup phase.
* Provide ongoing support to study teams and sites, addressing any issues that arise during the trial setup process.
Required Skills and Qualifications:
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* Bachelor's degree in a relevant field such as life sciences, clinical research, or healthcare management.
* Experience in clinical trial setup, regulatory submissions, or site management, preferably within the pharmaceutical or biotechnology industry.
* Strong understanding of clinical trial processes, regulatory requirements, and GCP guidelines.
* Excellent organizational skills and attention to detail, with the ability to manage multiple setup tasks simultaneously.
* Strong communication and interpersonal skills, with the ability to collaborate effectively with diverse teams and stakeholders.
Benefits:
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* Competitive salary and range of additional benefits focused on well-being and work-life balance opportunities.
* Annual leave entitlements and health insurance offerings to suit individual needs.
* Competitive retirement planning and global Employee Assistance Programme for employee and family support.
Why Work with Us:
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We are committed to fostering an inclusive and accessible environment for all candidates. Our success depends on the quality of our people, and we strive to build a diverse culture that rewards high performance and nurtures talent.