Clinical Research Associate Specialist
1 dia atrás
Job OverviewWe are seeking a highly skilled Clinical Research Associate to join our team.As a key member of the research team, you will play a pivotal role in the design and analysis of clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.Conduct onsite and remote monitoring activities in accordance with ICH-GCP guidelines, applicable regulations, SOPs, and study processes.Verify the protection of study participants by confirming informed consent procedures and protocol compliance with applicable regulations.E nsure the integrity of clinical data and adherence to approved protocols, GCP, regulations, and SOPs.Foster collaboration with investigative site staff to facilitate trial deliverables.Verify proper management and accountability of Investigational Product (IP).Prepare and submit reports of investigational site findings and update tracking systems.To be successful in this role, you will have a degree in a clinical, science, or health-related field from an accredited institution and prior experience supporting clinical trials, including solid on-site monitoring experience in CROs or pharma companies.Required Skills and QualificationsStrong understanding of ICH-GCP guidelines and applicable regulations.Excellent communication and interpersonal skills.Ability to work independently and as part of a team.Strong analytical and problem-solving skills.Proficient in MS Office and other relevant software applications.BenefitsThis is a great opportunity to contribute to the advancement of healthcare and make a meaningful impact.You will have the chance to work with a talented team of professionals who share your passion for research and innovation.About the RoleThis is a full-time position that offers competitive compensation and benefits.If you are a motivated and detail-oriented individual who is passionate about clinical research, we encourage you to apply.
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