Sobre este puesto de Clinical Research Associate II en Premier Research
You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success.
We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires.
Your ideas influence the way we work, and your voice matters here.
As an essential part of our team, you help us deliver the medical innovation that patients are desperate for.
Join us and build your future here.
What You'll be Doing:
Delivers quality, timely monitoring reports for sponsor approval per the Clinical Monitoring Plan timelines
Maintains submission of expenses according to travel and expense requirements within company guidelines
Monitors (remote, onsite, or other approved mode of monitoring) with a focus on data integrity and patient safety in accordance with specific country regulations
Plans day to day activities for monitoring of a clinical study and sets priorities per site
Prepares for and conducts on-site qualification, study initiation, interim monitoring, and close-out monitoring visits at investigator sites as required by clinical monitoring plan
Maintains Trial Master File (TMF)/electronic Trial Master File (eTMF) as defined by the organization’s processes per filing guidelines. Understands the required essential documents according to ICH/GCP Section 8.
Reviews site documents and verifies they are accurate, complete, current, and include required updates
What we are searching for:
Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (i.e., registered nurse); or equivalent work experience required
Previous clinical research experience required
At least 2+ years’ experience in clinical trials and independent monitoring
Experience working in one or more of the following therapy areas will be beneficial; Neurology, Oncology, Rare Diseases & Pediatrics
Preference at working across all phases I-IV, although phase II and III only will be considered
The role can be offered as fully remote, hybrid or office based. There will be an expectation for country-wide monitoring with the average frequency of days on site being 6 days per month.
