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Clinical Research Associate I
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Clinical Research Associate I
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Clinical Research Associate I
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Clinical Research Associate I(FSP)
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Clinical Research Associate I
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Clinical Research Associate I
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Clinical Research Associate
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Beijing, Beijing, China Parexel Full timeJob Summary:Parexel is seeking a skilled Clinical Research Associate to support our clinical trials. As a Clinical Research Associate, you will be responsible for ensuring the integrity and quality of our clinical trials, working closely with site staff, investigators, and other stakeholders.Key Responsibilities:Conduct site initiation, monitoring, and...
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Clinical Research Associate I
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Beijing, Beijing, China Parexel Full timeAbout the JobWe are seeking a highly skilled Clinical Research Associate I to join our team at Parexel. As a key member of our organization, you will be responsible for ensuring the overall integrity of study implementation and adherence to study protocol at clinical sites.Job DescriptionThe successful candidate will have experience in conducting site...
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Clinical Research Associate
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Clinical Research Associate I
2 weeks ago
Beijing, Beijing, China Parexel Full timeAbout the Role:Parexel is seeking a highly motivated and detail-oriented Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for ensuring the timely and accurate completion of project goals and updating applicable trial management systems.Key Responsibilities:Start-up Phase:Act as Parexel's direct point of...
Clinical Research Associate I
1 month ago
About the Role:
Parexel is seeking a highly motivated and detail-oriented Clinical Research Associate I to join our team. As a Clinical Research Associate I, you will be responsible for managing clinical trials from site identification through close-out, ensuring timely and accurate completion of project goals.
Key Responsibilities:- Start-up Phase: Act as Parexel's direct point of contact with assigned sites, accountable for quality and delivery during the start-up phase.
- Maintenance Phase: Ensure overall integrity of study implementation and adherence to study protocol at clinical sites, and perform problem-solving to address and resolve site issues.
- Overall Accountabilities: Ensure timely and accurate completion of project goals and update of applicable trial management systems.
- Education: Educated to degree level (biological science, pharmacy, or other health-related discipline preferred) or equivalent nursing qualification or other equivalent experience.
- Previous Experience: Previous relevant work experience preferred.
- Skills: Problem solving skills, ability to work independently, sound presentation skills, client-focused approach to work, ability to interact professionally within a client organization, flexible attitude with respect to work assignments and new learning, ability to manage multiple tasks, willingness to work in a matrix environment, strong computer skills, sound interpersonal, verbal, and written communication skills, sense of urgency in completing assigned tasks, and ability to assist others to meet study/country deliverables.
Parexel offers a dynamic and challenging work environment, opportunities for professional growth and development, and a competitive compensation package.