Senior Regulatory Medical Writer, Client-embedded, FSP

About the role

Our team of colleagues in clinical research services are at the forefront of getting cures to market. We bring a high caliber of scientific and clinical expertise to the development of drugs that address the world’s most challenging health concerns.

Responsibilities

• Conduct clinical trials and studies
• Collaborate with regulatory agencies and sponsors
• Manage clinical research projects from start to finish
• Ensure compliance with all relevant regulations and guidelines

Requirements

• Bachelor's degree in a related field
• Experience in clinical research or related field
• Strong organizational and project management skills
• Excellent communication and interpersonal skills

Qualifications

• Knowledge of clinical research protocols and standards
• Ability to work independently and as part of a team
• Proficiency in Microsoft Office Suite

Skills

• Strong analytical and problem-solving skills
• Attention to detail
• Ability to manage multiple tasks simultaneously

Benefits

• Flexible work schedule
• Health insurance coverage
• Retirement plan

Pay

Commensurate with experience

Schedule

TBD