Study Start Up Specialist (Clinical Research, Hybrid)

Job summary

The role involves overseeing clinical trial management workstreams, ensuring that deliverables meet quality and timeline expectations while contributing to the advancement of innovative treatments and therapies.

Qualifications

• Bachelor's degree in a relevant field.
• Minimum of [X] years of experience in clinical trial management.
• Proven expertise in designing and executing clinical trials with a strong understanding of regulatory requirements.
• Exceptional analytical and problem-solving skills, capable of interpreting complex medical data.
• Effective communication and interpersonal skills for collaboration across diverse teams.
• Detail-oriented and organized, with a history of managing multiple tasks and priorities.
• Willingness to travel as required (approximately 25%).

Responsibilities

• Collaborate with cross-functional teams to design and implement effective clinical trial enrollment.
• Oversee and manage the daily operations of clinical trials, ensuring compliance with regulatory standards.
• Analyze and interpret clinical trial data, identifying trends and providing insights to optimize study outcomes.
• Proactively address challenges and implement effective solutions for successful trial execution.
• Communicate effectively with internal and external stakeholders to foster partnerships and facilitate smooth trial processes.

Skills

• Strong analytical and problem-solving abilities.
• Excellent communication and interpersonal skills.
• Ability to manage competing priorities effectively.

Education

• Bachelor's degree in a relevant field.

Tools

• Familiarity with clinical trial management systems and data analysis tools.