Clinical Regulatory Strategy Consultant

Syner-G; United States; Remote; USD 75,000 - 90,000; Full time

Benefits offered by this job

Generous flexible paid time off program

Company-paid holidays

Flexible working hours

Job summary

Syner-G is looking for a Consultant II (Clinical Strategy) in the United States to guide clients through regulatory requirements. You will oversee the development and submission of regulatory documentation and work closely with clients in the drug development process.

The ideal candidate will have a strong background in drug development, along with excellent communication and strategic advice skills. This role offers flexible work options along with a supportive culture fostering professional growth.

Qualifications

• Bachelor’s degree in a relevant scientific discipline; MA degree preferred.
• RAC Certification is a significant advantage.
• Proficient in relevant software tools and understanding of drug development processes.

Responsibilities

• Oversee the preparation, review, and submission of regulatory documents.
• Engage in all phases of drug development.
• Serve as the main point of contact for clients and provide regulatory advice.

Skills

Strong background in drug development

Proven experience in handling INDs, NDAs, and BLAs

Excellent communication skills

Education

Bachelor’s degree in chemistry, pharmaceutics, or biology

MA degree preferred

Tools

Microsoft Office Suite

Trackwise

Veeva

ICTD

Job description

Syner-G is looking for a Consultant II (Clinical Strategy) in the United States to guide clients through regulatory requirements. You will oversee the development and submission of regulatory documentation and work closely with clients in the drug development process.

The ideal candidate will have a strong background in drug development, along with excellent communication and strategic advice skills. This role offers flexible work options along with a supportive culture fostering professional growth.