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Syneos Health
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Clinical Trial Manager

Clinical Trial Manager

Syneos Health

3 - 7 years

5 - 9 Lacs

Kolkata Mumbai New Delhi Hyderabad Pune Chennai Bengaluru

Posted:1 month ago| Platform:

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Skills Required

GCP Project management Analytical Clinical trials Agile Scheduling Life sciences Budgeting Recruitment Logistics

Work Mode

Work from Office

Job Type

Full Time

Job Description

Clinical Trial Manager

Job Responsibilities

Develop and coordinate Phase 1 clinical research studies, ensuring all aspects of the study are meticulously planned and executed
Implement clinical research protocols and ensure compliance with regulatory requirements, including Good Clinical Practice (GCP) guidelines
Collaborate with principal investigators, research subjects, client teams, and clinic operations teams to facilitate smooth communication and coordination
Plan and manage logistics and resource usage for clinical trials, including scheduling, budgeting, and resource allocation
Track study progress and ensure alignment with project milestones, client deliverables, and budget, providing regular updates to stakeholders
Prepare and present study reports and updates to stakeholders, including detailed analysis of study data and progress
Ensure adherence to global and regional regulations and guidelines, staying up-to-date with any changes or updates
Provide guidance and support to lower-level professionals and team members, fostering a collaborative and supportive work environment
Identify and resolve any issues or challenges that arise during the course of the study, ensuring timely and effective solutions
Maintain accurate and comprehensive documentation of all study-related activities, ensuring transparency and accountability

Qualifications:

Bachelors degree in a related field (e.g., life sciences, clinical research)
Minimum of 3 years of experience in clinical trial management or a related field
In-depth knowledge of clinical research processes and regulations
Strong project management and organizational skills
Excellent communication and interpersonal skills
Ability to work independently and as part of a team
Proficiency in using clinical trial management software and tools

Certifications:

Certified Clinical Research Professional (CCRP) or equivalent certification preferred

Necessary Skills:

Strong analytical and problem-solving skills
Attention to detail and accuracy
Ability to manage multiple projects and priorities simultaneously
Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)
Knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements

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