**Clinical Research Associate Role**
We are seeking a skilled Clinical Research Associate to play a key role in ensuring the success of our clinical trials. This individual will be responsible for performing site qualification, site initiation, interim monitoring, site management activities and close-out visits.
The ideal candidate will have a strong understanding of regulatory requirements, including ICH-GCP and Good Pharmacoepidemiology Practice (GPP). They will also possess excellent communication and interpersonal skills, with the ability to work effectively with study site personnel, investigators and Sponsor affiliates.
In addition to their technical skills, the successful candidate will be able to maintain a working knowledge of relevant regulations and company SOPs/processes. They will also be able to collaborate with cross-functional teams to ensure project objectives, deliverables and timelines are met.
* Responsibilities:
* Perform site qualification, site initiation, interim monitoring, site management activities and close-out visits.
* Evaluate overall performance of site and site staff.
* Maintain a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations and company SOPs/processes.
* Collaborate with study site personnel, investigators, and Sponsor affiliates to ensure project objectives, deliverables, and timelines are met.
This role requires a high level of accuracy, attention to detail and organizational skills. The successful candidate will be able to work independently and as part of a team to achieve project goals.