Clinical Trials Specialist
17 hours ago
Company Overview
Lifelancer is a leading talent-hiring platform in the Life Sciences, Pharma, and IT sectors. We connect professionals with opportunities in pharma, biotech, health sciences, healthtech, data science, and IT domains.
About Us
We are committed to revolutionizing the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Our team is dedicated to overcoming barriers in clinical trials and making a meaningful global impact.
Job Description
We are seeking a motivated problem-solver and creative thinker to join our team as a Clinical Trials Specialist - Regulatory Affairs. In this role, you will be responsible for undertaking primary medical review of cases, including medical assessment of the case for seriousness, listedness/labeling, causality, adverse event coding, and narrative review.
You will update and document daily case data, case-feedback in appropriate trackers/tools to facilitate tracking and workflow management. Additionally, you will assume complete responsibility for all assigned deliverables in line with expected quality, compliance, and productivity SLAs and KPIs.
Required Skills and Qualifications
- Strong knowledge of regulatory affairs and clinical trials processes
- Excellent communication and interpersonal skills
- Ability to work independently and as part of a team
- Proficiency in using various software tools and systems
Benefits
- Competitive salary: $85,000 per annum
- Ongoing training and professional development opportunities
- A collaborative and dynamic work environment
- The chance to make a meaningful global impact
Other Information
Please use the below Lifelancer link for job application and quicker response.
Apply Now
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