Clinical Research Monitoring Professional
2 semanas atrás
Clinical Research Associate II role available at a leading biopharmaceutical organization. The company translates unique clinical, medical affairs and commercial insights into outcomes to address modern market realities.
We are continuously looking for ways to simplify and streamline our work to make it easier to work with and easier to work for.
Collaborate with passionate problem solvers to help customers achieve their goals in a highly competitive and ever-changing environment.
Responsibilities- Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices.
- Develop and implement tools, procedures, and processes to ensure quality monitoring.
- Contribute to the design, implementation, and delivery of processes, programs, and policies.
- Manage defined components of projects or processes within the area of responsibility.
- Ensure accurate and timely documentation of monitoring activities and findings.
- Collaborate with cross-functional teams to support clinical trial operations.
- Bachelor's degree in a related field or equivalent experience.
- Minimum of 2-4 years of experience in clinical research monitoring.
- Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.
- Excellent communication and interpersonal skills.
- Ability to work independently and manage multiple priorities.
- Proficiency in using clinical trial management systems and other relevant software.
- Opportunity to work on 200+ studies across 73,000 sites and 675,000+ trial patients.
- A dynamic and challenging work environment.
- Chance to take the initiative and challenge the status quo.
The company has worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products over the past 5 years.
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