Informed Consent Writer

This is a fully remote position, open to applicants in Pennsylvania.

📋 Description

• Develop, write, and revise clinical study reports (CSRs), clinical protocols, investigator brochures (IBs), and patient narratives.

• Execute literature reviews, analyze data, and interpret results from clinical trials.

• Aid in the creation of scientific manuscripts, abstracts, and posters.

• Support the evaluation and verification of clinical data for precision, completeness, and alignment with study protocols, SOPs, and regulatory standards.

• Engage in project meetings, teleconferences, and client discussions.

• Review project goals, timelines, and expected outcomes.

• Offer insights and suggestions regarding document content, format, and presentation.

• Stay updated on emerging trends, scientific advancements, and regulatory changes in relevant therapeutic fields.

• Produce high-quality medical writing while collaborating closely with the team and stakeholders.

⛳️ Requirements

• Bachelor's degree in Life Sciences, Pharmacy, Medicine, or a related discipline.

• Strong interest in medical writing, clinical research, and the drug development process.

• Exceptional written and verbal communication abilities.

• Capability to convert complex medical and scientific information into clear, concise, and engaging content for varied audiences.

• Excellent attention to detail and strong organizational skills.

• Proficient in managing multiple tasks simultaneously, effectively prioritizing workload, and meeting project deadlines in a dynamic environment.

• Competence in Microsoft Office Suite (Word, Excel, PowerPoint).

• Familiarity with document management systems, reference management software, and statistical analysis tools is preferred.

• Ability to collaborate effectively as part of a multidisciplinary team.

• Skill in communicating effectively across various functional areas.

• Flexibility to adapt to changing project demands and priorities.

• Self-motivated individual with a desire for learning and professional advancement.

• Commitment to producing high-quality work and enhancing the success of clinical research projects.

• Legal authorization to work in the country where the position is located.

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Health and wellness programs including medical, dental, and vision coverage where applicable.

• Retirement and pension schemes.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

• Opportunities for learning and development through structured training and career paths.