Remote Clinical Research Associate II

Parexel; Poland; Remote; PLN 120,000 - 180,000; Full time

Job summary

Parexel is seeking an experienced Clinical Research Associate to join our Multi-Sponsor Clinical Trials Team in Poland. You will be the site’s sole point of contact, managing visits from site initiation to close-out while ensuring patient safety and data integrity.

The role offers exposure to world-class technology and training, with less travel and a bonus incentive program. You will advance your career in clinical research across multiple therapeutic areas with Parexel.

Qualifications

• Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology.
• Ability to perform all clinical monitoring activities independently.
• Experience with Oncology trials would be an advantage.
• Bachelor’s or equivalent degree in biological science, pharmacy or other health related discipline.
• Strong interpersonal, written, and verbal communication skills within a matrixed team.
• Experience working in a self-driven capacity, with a sense of urgency and limited oversight.
• The ability to manage multiple tasks, evaluate a variety of unpredictable scenarios and achieve project timelines while understanding study protocols.
• An honest and ethical work approach to promote the development of life changing treatments for patients.
• Strong computer skills, including CTMS, EDMS and MS-Office products such as Excel and Word.

Responsibilities

• Leverage your expertise. Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate visit/contact reports.
• Build relationships. Oversee integrity of the study and utilize problem-solving skills to promote rapport with the site and staff.
• Protect patients. Review the performance of the trial at designated sites, ensure the rights and well-being of human subjects are safeguarded and are in accordance with protocol.
• Drive productivity. Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines, while also ensuring compliance with SOPs, protocol/amendments, GCP, and applicable regulatory requirements.
• Ensure quality. Evaluate the quality and integrity of the reported data, site efficacy and drug accountability.
• Execute. Monitor the completeness and quality of Regulatory Documentation and perform site document verification.

Skills

Clinical research

Site management

CTMS

EDMS

MS Office

Oncology trials

Communication skills

Independent working

Client-focused

Education

Bachelor's degree in biological science or related health field

Tools

CTMS

EDMS

MS-Office

Job description

Parexel is seeking an experienced Clinical Research Associate to join our Multi-Sponsor Clinical Trials Team in Poland. You will be the site’s sole point of contact, managing visits from site initiation to close-out while ensuring patient safety and data integrity.

The role offers exposure to world-class technology and training, with less travel and a bonus incentive program. You will advance your career in clinical research across multiple therapeutic areas with Parexel.