Proposal Development Coordinator

About the role

Join Almac as a valued member of our team. We offer a unique culture that delivers exceptional solutions for Biopharma and Biotech. Our mission is to provide innovative solutions that drive progress in healthcare.

Responsibilities

• Contribute to the development and execution of clinical trial protocols.
• Manage and analyze clinical trial data using statistical software.
• Collaborate with cross-functional teams including regulatory affairs, clinical research, and project management.
• Prepare and present clinical trial reports to stakeholders.
• Ensure compliance with regulatory guidelines and sponsor requirements.

Requirements

• Bachelor's degree in Statistics, Biostatistics, or a related field.
• Minimum of 3 years of experience in clinical research and statistics.
• Proficiency in statistical analysis software such as SAS, R, or Python.
• Experience with regulatory submissions and Good Clinical Practice (GCP).
• Strong communication and interpersonal skills.
• Ability to work independently and as part of a team.

Qualifications

• Valid certification in Biostatistics or relevant field.
• Knowledge of clinical trial design and data management principles.
• Experience with electronic data capture systems (EDC).
• Understanding of clinical trial regulations and ethical considerations.

Skills

• Data analysis and interpretation.
• Statistical modeling and hypothesis testing.
• Project management and organizational skills.
• Attention to detail and ability to meet deadlines.
• Effective written and verbal communication skills.

Benefits

• Competitive salary package.
• Incentive bonuses based on performance.
• Vacation and holiday benefits.
• Paid training and professional development opportunities.
• Flexible working hours and remote work options.

Pay

Competitive salary commensurate with experience.

Schedule

Full-time position with standard business hours.