Study Nurse

Care Access; Warszawa; On-site; PLN 140,000 - 180,000; Full time

Benefits offered by this job

Paid Time Off

Medical, dental, and vision insurance

Job summary

Care Access is seeking a Study Nurse onsite in Poland to conduct delegated clinical tasks and monitor research participants in alignment with GCP. The role requires a nursing license, 1+ year of relevant experience, and skills in phlebotomy and IV procedures.

Responsibilities include IP preparation, regulatory compliance, data accuracy, and close collaboration with the study team and PI. Travel is minimal, and the position offers competitive benefits and professional growth.

Qualifications

• Active nursing qualification and registration in accordance with local regulatory requirements.
• A minimum of 1 year of relevant work experience required.
• Phlebotomy and infusion experience required.
• Clinical Research Experience preferred.

Responsibilities

• Clinical monitoring of participants per protocol; may include vital signs, cardiac rhythm, pulse oximetry.
• Phlebotomy and IV catheter insertion; process and ship labs; perform ECGs as required.
• Preparation and administration of Investigational Product (IP); proper storage and record-keeping.
• Regulatory compliance, safety and quality standards; maintain training and licensure.
• Team collaboration; attend meetings with study team and PI; maintain a clean work area.

Skills

Clinical nursing

Phlebotomy

Patient monitoring

Communication

Team collaboration

Problem solving

Education

Nursing degree

Job description

About Care Access

Care Access is working to make the future of health better for all. With hundreds of research locations, mobile clinics, and clinicians across the globe, we bring world-class research and health services directly to communities that often face barriers to care. We are dedicated to ensuring that every person has the opportunity to understand their health, access the care they need, and contribute to the medical breakthroughs of tomorrow.

With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress. Through partnerships, technology, and perseverance, we are reimagining how clinical research and health services reach the world. Together, we are building a future of health that is better and more accessible for all.

The Study Nurse conducts delegated clinical tasks and monitoring of research participants in accordance with Good Clinical Practices (GCP), ensuring protocol and regulatory compliance.

• Participant Care, Monitoring & Clinical Assessments
  • Clinical Monitoring of participants, per protocol. This may include monitoring vital signs, cardiac rhythm strips, pulse oximetry, etc.
  • Monitoring of participant for adverse reactions.
  • Conduct delegated clinical procedures as required per protocol.
  • Treat patients with standing orders for anaphylactic reactions.
  • Communicate regularly with the Principal Investigator (PI).
• Clinical Procedures, Phlebotomy & Specimen Management
  • Perform phlebotomy and insert IV catheters, as required.
  • Process and ship labs (independently or with limited supervision).
  • Performing electrocardiograms (independently or with limited supervision).
• Investigational Product (IP) Management
  • Preparation and administration of Investigational Product (IP; study drug).
  • Receipt and proper storage of investigational products.
  • Maintain Investigational Product records in accordance with regulations and sponsor requirements.
  • Maintain the blind of all study products where required.
  • Maintain proper storage, security and temperature for all medications and investigational products.
• Regulatory Compliance, Quality & Safety
  • Comply with regulatory requirements, policies, procedures, and standards of practice.
  • Comply with Safety and PPE standards.
  • Maintain appropriate research training and nursing licensure in good standing.
• Study Team Collaboration & Operational Support
  • Attend and participate in meetings with direct manager and study team.
  • Communicate regularly with the Principal Investigator (PI).
  • Maintain a clean work area.
• Other Responsibilities
  • Maintain a clean work area.
  • Attend and participate in meetings with direct manager and study team.
  • Maintain appropriate research training and nursing licensure in good standing.
  • Perform other duties consistent with the scope and level of the role as assigned
• Ability to communicate and work effectively with a diverse team of professionals.
• Team Collaboration Skills: Work effectively and collaboratively with other team members toaccomplishmutual goals. Bringpositiveand supportive attitude to achieving these goals.
• Ability to work independently in a fast-paced environment with minimal supervision.
• Strong organizational skills: Able to prioritize, delegate, direct, support, assign and evaluateotherswork and follow through on assignments.
• Communication Skills: Strong verbal and written communication skills asevidencedby positive interactions with coworkers, management, clients, and vendors.
• Team Collaboration Skills: Work effectively and collaboratively with other team members toaccomplishmutual goals. Bringpositiveand supportive attitude to achieving these goals.
• Ability to balance tasks with competing priorities.
• Critical thinker and problem solver.
• Curiosity and passion to learn, innovate, able to take thoughtful risks and get things done.
• Friendly, outgoing personality;maintaina positive attitude under pressure.
• High levelof self-motivation and energy.
• Must have a client service mentality.
• Active nursing qualification and registration in accordance with local regulatory requirements.
• A minimum of 1 year of relevant work experiencerequired.
• Phlebotomy and infusion experiencerequired.
• Clinical Research Experience preferred.
• Location: Onsite within Poland
• Travel: Minimal (<10%), planned in advance.
• Physical Requirements:Walking -15%, Standing - 10%, Sitting - 70%, Lifting up to, over, and overhead 25 lbs - 5%

The expected pay range for this role is $140,000 - $180,000 PLN per year for full time team members.

• Paid Time Off (PTO) and Company Paid Holidays
• Medical, dental, and vision insurance plan options

Privacy Notice

By applying for this position, you acknowledge that Care Access will collect and process the personal information you submit as part of the recruitment process. Your personal information may be accessed, transferred to, stored, and processed in the United States and other countries where Care Access and its service providers operate, subject to appropriate safeguards where required by applicable law. To learn more about how we collect, use, disclose, retain, privacy rights, and otherwise process applicantinformation, please review our Privacy Policy: https://careaccess.com/privacy-policy .

We work with and serve people from diverse cultures and communities around the world. We are stronger and better when we build a team representing the communities we support. We maintain an inclusive culture where people from a broad range of backgrounds feel valued and respected as they contribute to our mission.

We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to, and will not be discriminated against on the basis of, race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.

Care Access is unable to sponsor work visas at this time.

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