Clinical Research Associate, Single Sponsor dedicated in Poland
IQVIA
Clinical Research Associate, Single Sponsor dedicated in Poland
Job Description
IQVIA is hiring Clinical Research Associates!Join IQVIA today and make an impact on patients’ outcome!Job OverviewPerform 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.ResponsibilitiesPerforming site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentationSupporting the development of a subject recruitment planEstablishing regular lines of communication plus administering protocol and related study training to assigned sitesEvaluating the quality and integrity of site practices – escalating quality issues as appropriateManaging progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution QualificationsMinimum 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 #fspcaresIQVIA 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.comIQVIA 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 119.400,00 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.
Locations
- Poland, Warsaw
- Poland, Warsaw
Skills Required
- use of Microsoft Wordintermediate
Required Qualifications
- Minimum of a Bachelors Degree in scientific discipline or health care. (degree in scientific discipline or health care)
- Experience of 1 year in on-site monitoring clinical trials. (experience, 1 years)
- 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). (experience)
- Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable). (experience)
- Written and verbal communication skills including good command of Polish and English language. (experience)
- Ability to establish and maintain effective working relationships with co-workers, managers, and clients. (experience)
- Minimum of a Bachelors Degree in scientific discipline or health care. (degree in scientific discipline or health care)
- Experience of 1 year in on-site monitoring clinical trials. (experience, 1 years)
- 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). (experience)
- Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable). (experience)
- Written and verbal communication skills including good command of Polish and English language. (experience)
- Ability to establish and maintain effective working relationships with co-workers, managers, and clients. (experience)
- Connect to great opportunity™ (experience)
- 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. (experience)
- #weareIQVIA #projectpatientfocus #LI-Remote #CRASDAJD #CRA #fspcares (experience)
- 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 (experience)
- 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. (experience)
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
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