Assistant Clinical Research Manager

Job Overview

We are seeking a highly motivated and detail-oriented Assistant Clinical Research Manager to join our dynamic research team. In this vital role, you will support the planning, execution, and oversight of clinical trials, ensuring adherence to regulatory standards and ethical guidelines. Your energetic approach will help drive research projects forward, facilitate compliance, and maintain high-quality data collection. This position offers an exciting opportunity to contribute to groundbreaking healthcare advancements while developing your expertise in clinical research management.

Responsibilities

Assist in coordinating all phases of clinical trials, from protocol development to study completion, ensuring timely progress and compliance with regulatory standards.
Supervise research staff and study coordinators, providing guidance on clinical procedures, documentation review, and data collection methods, and at the same time, step in as study coordinator when needed.
Monitor patient safety and well-being throughout the trial process, including blood sampling, patient monitoring, and adverse event reporting.
Review study documentation for accuracy and completeness, ensuring adherence to FDA regulations, ICH GCP guidelines, and clinical ethical standards.
Manage data entry and analysis using statistical software and ensure data management practices align with CDISC standards.
Oversee compliance with healthcare regulations and clinical quality assurance standards across all research activities.
Collaborate with cross-functional teams to ensure proper use of EMR systems and adherence to project timelines in a fast-paced research setting.

Experience

Proven supervising experience in a clinical research environment or healthcare setting.
Strong knowledge of medical terminology, clinical laboratory procedures, and blood sampling techniques.
Experience reviewing documentation for accuracy and compliance within clinical trials or research projects.
Familiarity with statistical software tools used for data analysis in clinical studies.
Understanding of FDA regulations, ICH GCP guidelines, and healthcare compliance standards related to clinical research.
Hands-on experience with EMR systems, project management tools, and data management platforms such as CDISC standards.
Certification in ICH GCP (Good Clinical Practice) from a recognized issuer is required; valid CA certification is preferred for applicable regions.
Demonstrated ability to manage multiple projects simultaneously while maintaining attention to detail and quality assurance standards.
Minimum 2 to 5 years clinical research experience
Foreign Medical Graduate or Bachelor's Degree

Join us in advancing healthcare through innovative research! We are committed to fostering a collaborative environment where your skills can thrive while making a meaningful impact on patient care worldwide. All roles are paid positions that support your professional growth within a vibrant research community dedicated to excellence.

Pay: $29.00 - $33.00 per hour

Benefits: