Clinical Research Associate, Single Sponsor dedicated in Poland

IQVIA Argentina; Warszawa; Hybrid; PLN 133,000 - 280,000; Full time

Job summary

IQVIA is hiring Clinical Research Associates to monitor sites and manage study activities, ensuring compliance with the protocol, GCP, ICH guidelines, and sponsor requirements. You will perform site visits, initiate, monitor, and close-out activities, and support data integrity across study sites.

The role requires a Bachelor's degree in a scientific field or health care, plus at least one year of on-site monitoring experience and strong communication in Polish and English.

Qualifications

• Bachelor's degree in scientific discipline or health care.
• Minimum 1 year on-site monitoring clinical trials.
• Good knowledge of, and skill in applying, GCP and ICH guidelines.
• MS Office proficiency (Word, Excel, PowerPoint) and use of laptop/iPhone/iPad where applicable.
• Written and verbal communication skills including good command of Polish and English.
• Ability to establish and maintain effective working relationships with co-workers, managers, and clients.

Responsibilities

• Perform site selection, initiation, monitoring and close-out visits, plus maintaining documentation.
• Support the development of a subject recruitment plan.
• Establish regular communication and administer protocol training to assigned sites.
• Evaluate the quality and integrity of site practices – escalating quality issues as appropriate.
• Managing progress by tracking regulatory submissions, recruitment, CRF completion, and data query resolution.

Skills

Communication skills

Relationship building

Regulatory knowledge (GCP/ICH)

On-site monitoring

Education

Bachelor's degree in scientific discipline or health care

Tools

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Job description

IQVIA is hiring Clinical Research Associates!

Join IQVIA today and make an impact on patients’ outcome!

Job Overview

Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Responsibilities

• Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
• Supporting the development of a subject recruitment plan
• Establishing regular lines of communication plus administering protocol and related study training to assigned sites
• Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
• Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution

Qualifications

• Minimum of a Bachelors Degree in scientific discipline or health care.
• Experience of 1 year in on-site monitoring clinical trials.
• Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).
• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
• Written and verbal communication skills including good command of Polish and English language.
• Ability to establish and maintain effective working relationships with co-workers, managers, and clients.

Connect to great opportunity

IQVIA is a strong advocate of diversity and inclusion in the workplace. We believe that a work environment that embraces diversity will give us a competitive advantage in the global marketplace and enhance our success. We believe that an inclusive and respectful workplace culture fosters a sense of belonging among our employees, builds a stronger team, and allows individual employees the opportunity to maximize their personal potential.

#weareIQVIA #projectpatientfocus #LI-Remote #CRASDAJD #CRA #fspcares

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is 132.800,00 zł - 280.000,00 zł. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.