Senior Clinical Research Associate
hace 1 mes
We are seeking a highly experienced and skilled Senior Clinical Research Associate to join our team as a Site Relationship Manager. This role will be responsible for building and maintaining strong relationships with clinical sites, ensuring their success and quality delivery.
As a Senior CRA, you will have at least 7 years of experience in clinical research and possess advanced English language skills. Your expertise will enable you to work independently, manage multiple tasks, and apply your understanding of study protocols to achieve project timelines.
Key Responsibilities- Leverage your expertise to generate and review visit/contact reports.
- Build relationships by overseeing the integrity of the study and utilizing problem-solving skills to promote rapport with the site and staff.
- Protect patients by reviewing the performance of the trial at designated sites, ensuring their rights and well-being are safeguarded and in accordance with protocol.
- Drive productivity by developing patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines, while ensuring compliance with approved standard operating procedures (SOPs), protocol/amendment(s), GCP, and applicable regulatory requirements.
- Ensure quality by evaluating the quality and integrity of reported data, site efficacy, and drug accountability.
- Execute by monitoring the completeness and quality of Regulatory Documentation and performing site document verification.
- At least 7 years of CRA experience.
- Proficient in English.
- 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 self-driven, 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 unpredictable scenarios, and achieve project timelines while applying 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 knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS), and MS-Office products such as Excel and Word.
The estimated salary range for this role is between $80,000 and $120,000 per year, depending on experience and qualifications. Additionally, you can expect a comprehensive benefits package, including health insurance, retirement plan, and paid time off.
About ParexelParexel is a leading global biopharmaceutical services company that provides a wide range of solutions to help clients succeed in the pharmaceutical and biotechnology industries. We offer a dynamic and supportive work environment, with opportunities for career growth and professional development. Our company values include integrity, collaboration, and innovation, and we strive to make a positive impact on people's lives through our work.
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