Remote Monitoring Specialist
We are seeking a skilled Remote Monitoring Specialist to oversee and ensure the integrity of clinical research studies by monitoring data and processes from a centralized location.
The successful candidate will conduct remote monitoring of trial sites to verify compliance with regulatory requirements and clinical protocols. They will utilize data analytics and risk-based monitoring techniques to identify potential issues and trends, ensuring that trials are conducted in accordance with established clinical practices.
The primary responsibilities of this role include:
* Site qualification, initiation, interim monitoring, site management activities, and close-out visits
* Verifying informed consent and protecting subject/patient confidentiality
* Conducting source document review and verifying required clinical data
* Applying query resolution techniques remotely and on-site
* May perform investigational product inventory, reconciliation, and reviews storage and security
This is an excellent opportunity for professionals who possess strong analytical skills, attention to detail, and ability to work independently in a fast-paced environment. The ideal candidate will be able to communicate effectively with cross-functional teams and provide high-quality results in a timely manner.
Responsibilities:
* Verify compliance with regulatory requirements and clinical protocols
* Utilize data analytics and risk-based monitoring techniques
* Identify potential issues and trends
* Ensure trials are conducted in accordance with established clinical practices
* Maintain accurate records and reports
Requirements:
* Strong analytical skills and attention to detail
* Ability to work independently in a fast-paced environment
* Effective communication skills
* Experience with data analytics and risk-based monitoring techniques
* Knowledge of clinical protocols and regulatory requirements