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88,000+ live jobsClinical Research Associate II
Remote from Spain·Full-time·Added 12 days ago (last checked 9 Nov)
8 open roles
Our summary
- Work mode
- Remote from Spain
- Contract
- Full-time
- Experience
- 2+ years
- Education
- University degree
Visa options
The ad doesn’t mention sponsorship
Not a refusal, but not a yes. Worth asking in your first message.
Skills
Requirements
What we're looking 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 Dermatology therapy area required
Nice to have
- Preference at working across all phases I-IV, although phase II and III only will be considered
The role
Premier Research is looking for a Clinical Research Associate II to join our Clinical Monitoring, Site Management and SSU team.
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.
As an essential part of our team, you help us deliver the medical innovation that patients are desperate for.
What you'll do
- 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
How you'll work
The role can be offered as fully remote, hybrid or office based, from Madrid. There will be an expectation for country-wide monitoring with the average frequency of days on site being 6 days per month.
About Premier Research
- Industry
- Pharma
In their own words
About the company & team
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.
Join us and build your future here.
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