Contribute to impactful clinical trials in a hybrid work environment. Collaborate with leading professionals in a science-driven organization. Enhance your expertise in clinical study management systems.
Clinical Study Specialist
in Healthcare + Life Sciences ContractJob Detail
Job Description
Overview
- Provide technical and administrative support to clinical study teams executing clinical trials.
- Assist in the execution of multiple studies across clinical programs.
- Support both internally sourced studies and those outsourced to Clinical Research Organizations (CROs).
- Contribute to a fast-growing, science-driven organization impacting patient care globally.
- Collaborate with Clinical Study Leads and Associate Managers to ensure study success.
- Hybrid work arrangement with onsite presence required four days a week.
- Engage in a six-month contract role with opportunities for professional growth.
- Utilize industry-standard tools and methodologies to support clinical trial management.
Key Responsibilities & Duties
- Organize and deliver reports and metrics to clinical study leads.
- Schedule and coordinate meetings, prepare agendas, and document minutes.
- Collate data for feasibility assessments and site selection processes.
- Review and facilitate study document approvals per standard operating procedures.
- Compile and maintain study manuals and reference materials.
- Track site activation, enrollment, and monitoring visits against plans.
- Perform reconciliations of study Trial Master File (TMF) and scheduled reporting.
- Monitor study close-out activities, including document and visit tracking.
Job Requirements
- Bachelor’s degree in Science and 2+ years of industry-related clinical experience.
- Proficiency in trial management systems and MS applications like Project, PowerPoint, Word, and Excel.
- Basic familiarity with medical terminology and clinical drug development processes.
- Strong attention to detail and ability to track and deliver study activities.
- Effective communication and interpersonal skills for internal and external collaboration.
- Resourceful problem-solving skills and proactive information assessment capabilities.
- Knowledge of ICH/GCP guidelines and clinical trial standards.
- Self-disciplined with strong time management and prioritization abilities.
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