Clinical Research Associate

Premier Research; Poland; Remote; PLN 102,000 - 124,000; Full time

Benefits offered by this job

Health insurance

Life insurance

Retirement plan

Paid time off

Employee Assistance Program

Job summary

Premier Research is seeking a Clinical Research Associate to join our Clinical Monitoring, Site Management and SSU team. This role helps transform ideas into medicines, ensuring patient safety and high-quality data across studies.

You will plan site visits, support Phase II and III trials, and collaborate with cross-functional teams to ensure regulatory compliance. Fully or partly remote options available for applicants in Poland.

Qualifications

• Undergraduate degree or international equivalent in clinical, science, or health-related field.
• Licensed health-care professional (e.g., registered nurse) or equivalent work experience.
• 1 year of independent monitoring experience in clinical research.
• Experience across therapy areas: Neurology, Oncology, Dermatology.
• Experience supporting Phase II & III studies.

Responsibilities

• Delivers quality, timely monitoring reports per the Clinical Monitoring Plan timelines.
• Maintains submission of expenses per travel and expense requirements.
• Monitors remotely, onsite, or other approved mode with focus on data integrity and patient safety per country regulations.
• Plans day-to-day monitoring activities and sets site priorities.
• Prepares for and conducts on-site visits (qualification, initiation, interim monitoring, close-out).
• Maintains TMF/eTMF per filing guidelines and understands essential documents per ICH/GCP Section 8.
• Reviews site documents for accuracy and updates.

Skills

Clinical monitoring

Data integrity

Regulatory compliance

Cross-functional collaboration

Education

Undergraduate degree in clinical/science/health

Tools

eTMF

Job description

Premier Research is looking for a Clinical Research Associate 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.

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.

• 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.

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 to include at least 1 year of independent monitoring
• Experience working ideally across all, if not some, of the following therapy areas; Neurology, Oncology, and Dermatology
• Experience at supporting Phase II & III studies.

The role can be offered as fully remote and applications will ideally be based in central Poland.

Premier Research is dedicated to providing compensation that is fair and competitive with market standards. The minimum annualized starting base pay for this role is 113,000 PLN. The actual salary will be influenced based on a variety of factors such as qualifications, skills, competencies, and proficiency for the role.

• health insurance
• life insurance
• retirement plan
• paid time off
• Employee Assistance Program