Clinical Trial Manager

Job Responsibilities

• Develop and coordinate Phase 1 clinical research studies, ensuring detailed planning and flawless execution.
• Implement clinical research protocols while ensuring compliance with Good Clinical Practice (GCP) and other regulatory requirements.
• Collaborate with principal investigators, research subjects, client teams, and clinic operations teams to ensure smooth study execution.
• Plan and manage logistics, scheduling, budgeting, and resource allocation for clinical trials.
• Track study progress against milestones, deliverables, and budgets, and provide regular updates to stakeholders.
• Prepare and present study reports, data analyses, and progress updates to clients and internal teams.
• Ensure adherence to global and regional regulations while staying updated with any regulatory changes.
• Provide guidance and mentorship to junior team members, fostering collaboration.
• Identify and resolve issues or risks during the study, ensuring timely corrective actions.
• Maintain comprehensive documentation of all study-related activities.

Qualifications

• Bachelor's degree in Life Sciences, Clinical Research, or a related field.
• 3+ years of experience in clinical trial management or related field.
• Strong knowledge of clinical research processes, GCP, and regulatory requirements.
• Proven project management and organizational skills.
• Excellent communication and interpersonal skills with ability to work independently and in teams.
• Proficiency with clinical trial management systems (CTMS) and tools.

Preferred Certifications

• Certified Clinical Research Professional (CCRP) or equivalent preferred.

Skills Required

• Strong analytical and problem-solving abilities.
• High attention to detail and accuracy.
• Ability to manage multiple projects and priorities simultaneously.
• Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).