Clinical Research Associate II
Parexel
full-time
Posted on:
Location Type: Remote
Location: United Kingdom
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Tech Stack
About the role
- Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate visit/contact reports
- Oversee integrity of the study and utilize problem-solving skills to promote rapport with the site and staff
- 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
- Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines, while also ensuring compliance with the approved standard operating procedures (SOPs), protocol/amendment(s), GCP, and the applicable regulatory requirement(s)
- Evaluate the quality and integrity of the reported data, site efficacy and drug accountability
- Monitor the completeness and quality of Regulatory Documentation and perform site document verification
Requirements
- Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology
- Ability to perform all clinical monitoring activities independently
- 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
- A client-focused approach to work and flexible attitude with respect to assignments/new learning
- The ability to manage multiple tasks, evaluate a variety of unpredictable scenarios and achieve project timelines while being able to apply your understanding of study protocol(s)
- An honest and ethical work approach to promote the development of life changing treatments for patients
- Strong computer skills, including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS) and MS-Office products such as Excel and Word.
Benefits
- world class technology and training
- bonus incentive program
- opportunity to work within multiple therapeutic areas
- opportunity to advance your career in clinical research
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical trials methodologyclinical monitoring activitiespatient recruitment strategiesdata quality evaluationregulatory documentation verificationdrug accountability
Soft Skills
problem-solvinginterpersonal communicationwritten communicationverbal communicationself-drivenclient-focusedflexibilitytask managementethical work approach