Competitive salary; not specified; benefits includ...
Bachelor's degree in scientific discipline
Proficiency in interpreting complex clinical data
Strong understanding of ich-gcp and fda regulations
The role involves leading the preparation, review, and editing of clinical study documents such as protocols and reports while ensuring accuracy and clarity
Job Summary
The role involves leading the preparation, review, and editing of clinical study documents such as protocols and reports while ensuring accuracy and clarity.
Candidates will collaborate closely with cross-functional teams including biostatistics and regulatory affairs to interpret clinical trial data and summarize findings.
ICON offers a competitive salary, diverse benefits including health insurance and retirement planning, and a commitment to an inclusive workplace culture.
Matching Summary
The role involves leading the preparation, review, and editing of clinical study documents such as protocols and reports while ensuring accuracy and clarity.
Salary
Competitive salary; Not specified; Benefits include annual leave, health insurance, retirement planning, and global assistance program
Skills & Requirements
Must-have
Bachelor's degree in scientific discipline
Proficiency in interpreting complex clinical data
Strong understanding of ICH-GCP and FDA regulations
Experience with regulatory submissions and publications
Ability to manage multiple projects simultaneously
Nice-to-have
Mentoring and coaching junior medical writers
Excellent interpersonal and communication skills
Strategic input on clinical development programs
Collaboration with cross-functional teams
Culture of excellence and continuous learning
Key Requirements
Bachelor's degree in relevant scientific or healthcare field
Proficiency in regulatory requirements (ICH-GCP, FDA, EMA)
Demonstrated ability to work in fast-paced environment