Job Title:
Senior Clinical Research Associate
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Job Description:
* As a Senior Clinical Research Associate, you will play a crucial role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.
You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.
Key Responsibilities:
1. Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
2. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
3. Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
4. Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
5. Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.
Requirements:
* Advanced degree in a relevant field such as life sciences, nursing, or medicine.
* Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
* Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
* Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
* Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
What We Offer:
* A competitive salary and benefits package.
* Opportunities for professional growth and development.
* A dynamic and supportive work environment.
* Recognition and rewards for outstanding performance.