Clinical Research Specialist
3 weken geleden
Are you ready for an exciting role as a Clinical Research Specialist, where you will be responsible for conducting clinical studies in compliance with applicable clinical and regulatory standards and in alignment with Medtronic business needs? You will monitor progress and results of clinical investigations in preparation for device application and/or publications. You will be responsible for managing and meeting the objectives of a clinical study. Assumes project management responsibilities for selected studies and site management activities as needed.
A Day in the LifeResponsibilities may include the following and other duties may be assigned.
- Assist in designing, planning, and developing clinical evaluation research studies for products that are under Clinical Investigation.
- Prepares and authors protocols and patient record forms.
- Conducts registered and non-registered clinical studies of products that have been determined to satisfy a medical need and/or offer a commercial potential.
- Oversees and interpret results of clinical investigations in preparation for new device or consumer application.
- Oversees and manages operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP) and specific country regulations, and may prepare clinical trial budgets.
- Serves as liaison between program management and planning, study team, and leadership.
- Collaborates and partners with a cross-functional team which includes site managers, monitoring, safety, stats, and others
- Assist in reviewing status of projects and budgets; manages schedules and prepares status reports.
We are looking for a highly motivated and experienced Clinical Research Specialist to join our team. The ideal candidate will have a Bachelor's degree in a relevant field and a minimum of 2 years of clinical research experience, or a Master's degree/PhD with 0 years of experience.
Preferred QualificationsWe prefer candidates with a degree in engineering, life sciences, or a related medical/scientific field. Experience in Good Clinical Practice (GCP) and/or regulatory compliance guidelines for clinical trials is also desirable. Additionally, experience managing multiple clinical research sites with proven results in study execution, clinical operations, and clinical strategy development is a plus.
What We OfferWe offer a competitive salary and benefits package to all our employees, including a flexible working environment, annual incentive plan, pension scheme, group discount on healthcare insurance, training possibilities, and employee assistance program.
Our CommitmentWe are committed to inclusion, diversity, and equity, and we strive to create a workplace where all employees belong, are respected, and feel valued for who they are and the life experiences they contribute. We believe that equity starts beyond our workplace and we must play a role in addressing systemic inequities in our communities to have long-term sustainable impact.
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