Clinical Research Associate - IQVIA Biotech Poland
Welcome to IQVIA, a global leader in healthcare data, technology, and services. We are currently seeking a talented and dedicated Clinical Research Associate to join our growing team at IQVIA Biotech Poland. As a Clinical Research Associate, you will play a vital role in our mission to accelerate the development of life-changing therapies for patients around the world. We are looking for someone with a strong background in clinical research, excellent communication and organization skills, and a passion for improving the lives of patients through innovative research. If you are driven, detail-oriented, and eager to contribute to groundbreaking research, we encourage you to apply for this exciting opportunity.
Conduct clinical research activities in compliance with applicable regulations and protocols.
Assist in the development and review of clinical trial documents, including protocols, informed consent forms, and study reports.
Perform site selection, initiation, monitoring, and close-out visits at investigator sites.
Ensure timely and accurate data collection, documentation, and reporting.
Communicate with study team members, investigators, and site staff to ensure adherence to study protocols and timelines.
Identify and resolve study issues and protocol deviations.
Maintain study files and records in accordance with company and regulatory requirements.
Participate in the development and review of Standard Operating Procedures (SOPs) and study-specific procedures.
Collaborate with cross-functional teams to ensure study milestones and deliverables are met.
Participate in the training and mentoring of new team members.
Keep abreast of industry trends, regulations, and guidelines related to clinical research.
Provide support for regulatory submissions and inspections.
Contribute to process improvement initiatives to enhance study efficiency and quality.
Represent IQVIA at investigator meetings, conferences, and other external meetings as needed.
Demonstrate a commitment to quality, integrity, and ethical conduct in all job responsibilities.
IQVIA is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
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Conduct clinical research activities in compliance with applicable regulations and protocols.
Assist in the development and review of clinical trial documents, including protocols, informed consent forms, and study reports.
Perform site selection, initiation, monitoring, and close-out visits at investigator sites.
Ensure timely and accurate data collection, documentation, and reporting.
Communicate with study team members, investigators, and site staff to ensure adherence to study protocols and timelines.
Identify and resolve study issues and protocol deviations.
Maintain study files and records in accordance with company and regulatory requirements.
Participate in the development and review of Standard Operating Procedures (SOPs) and study-specific procedures.
Collaborate with cross-functional teams to ensure study milestones and deliverables are met.
Participate in the training and mentoring of new team members.
Keep abreast of industry trends, regulations, and guidelines related to clinical research.
Provide support for regulatory submissions and inspections.
Contribute to process improvement initiatives to enhance study efficiency and quality.
Represent IQVIA at investigator meetings, conferences, and other external meetings as needed.
Demonstrate a commitment to quality, integrity, and ethical conduct in all job responsibilities.
IQVIA is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
Apply tot his job
Apply To this Job