Clinical Scientist – Medical Writing | Remote, Canada
Location: Canada (Remote; Option to work from Montreal HQ)
Employment Type: Permanent, Full-Time
Professional Level: Mid-Senior
About the Role
Indero, a leading contract research organization (CRO) specializing in dermatology, is seeking a Clinical Scientist to drive medical writing initiatives and support clinical development programs across all phases of clinical research. The Clinical Scientist will author and review clinical and regulatory documents, including study protocols, statistical analysis plans, clinical study reports, and scientific publications, ensuring high-quality, accurate, and compliant deliverables aligned with ICH-GCP, Health Canada, and FDA regulations.
This role is ideal for a medical writer with proven expertise in clinical research documentation, a passion for staying current in the scientific landscape, and a desire to make a tangible impact in a growing CRO.
Key Responsibilities
Medical Writing & Documentation
Own medical writing deliverables, ensuring scientific accuracy, compliance, and adherence to timelines.
Write and review study protocols, protocol amendments, informed consent/assent forms, study reference manuals, statistical analysis plans, and mock shells for tables/figures/listings.
Prepare clinical study reports, narratives, scientific abstracts, posters, and manuscripts.
Analyze, interpret, and summarize study data based on scientific expertise and industry standards.
Conduct online literature reviews to support document development and scientific communication.
Perform quality control reviews of documents prepared by other team members.
Collaboration & Process Improvement
Contribute to clinical development strategies across Phase 1 (FIM), Proof of Concept (POC), Phase 2b–3, and Phase 4/registry trials.
Collaborate with cross-functional teams, including clinical operations, biostatistics, and regulatory affairs, to ensure seamless integration of scientific content.
Participate in departmental process improvement initiatives to enhance documentation quality and efficiency.
Required Qualifications
Education
Master’s degree in Life Sciences; PhD preferred.
Experience
Minimum 3–5 years of experience in clinical and regulatory medical writing for clinical trials.
Experience developing study protocols, clinical study reports, and statistical analysis documentation.
Demonstrated ability to analyze and interpret clinical study data to support medical writing deliverables.
Knowledge & Skills
Strong understanding of drug development processes, clinical trial methodology, and regulatory requirements (Health Canada, FDA, ICH-GCP).
Advanced proficiency in scientific writing in English; French language skills are an asset.
Proficiency in Microsoft Word and other document management tools.
Excellent attention to detail, organizational skills, and ability to manage multiple projects simultaneously.
Strong problem-solving skills, adaptability, and client-focused attitude.
Ability to work independently in a remote or hybrid environment.
Work Environment & Benefits
Flexible work schedule with the option to work remotely anywhere in Canada or from Montreal headquarters.
Permanent full-time position with comprehensive benefits: medical, dental, vision, RRSP, vacation, personal days, virtual medical clinic, public transportation rebates, and social activities.
Professional development and ongoing training opportunities to enhance clinical and regulatory expertise.
Dynamic and collaborative team environment emphasizing innovation, reliability, and responsiveness.
About Indero
Indero, formerly Innovaderm, is a global CRO specializing in dermatology with over 20 years of experience in clinical research. We provide full-service clinical trial solutions from protocol development and patient recruitment to trial monitoring and biostatistics, serving biotech and pharmaceutical sponsors worldwide. Headquartered in Montreal, we operate across North America and Europe, with a strong reputation for high-quality research and client satisfaction.
Indero is committed to equitable treatment and equal opportunity. Accommodations are provided for candidates with disabilities during the recruitment process. Only candidates legally authorized to work in Canada will be considered.
Apply Now
Join Indero as a Clinical Scientist and play a pivotal role in medical writing and clinical research innovation, shaping the future of dermatology clinical trials.
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