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Clinical Research Associate Ii / Associé De Recherche Clinique Ii, Bilingue, Montreal, Canada

Indero
Indero
1-3 years
Not Disclosed
10 Jan. 5, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Bilingual Clinical Research Associate II – Dermatology & Rheumatology

Location: Montreal, Canada (Remote work optional within Canada)
Employment Type: Permanent, Full-Time
Professional Level: Mid-Senior (CRA II)


About the Role

Indero, a leading contract research organization (CRO) specializing in dermatology and rheumatology, is seeking a Bilingual Clinical Research Associate II (CRA II) to monitor clinical study progress at investigative sites or remotely. The CRA II ensures that all clinical trials are executed, documented, and reported in full compliance with protocols, Standard Operating Procedures (SOPs), ICH-GCP guidelines, and regulatory requirements.

This role is ideal for a bilingual CRA who thrives in autonomous environments, seeks to grow their expertise in dermatology, and values working in a mid-sized, collaborative CRO where individual contributions are recognized and impactful.


Key Responsibilities

Clinical Monitoring

  • Conduct site qualification, initiation, monitoring, and close-out visits in accordance with the monitoring plan, sponsor and CRO SOPs, ICH-GCP guidelines, and applicable regulations.

  • Perform source data verification (SDV), ensure proper storage, dispensing, and accountability of study drugs, and maintain accurate regulatory documentation.

  • Participate in investigator meetings and maintain strong, productive relationships with site staff to support study objectives and patient recruitment targets.

  • Prepare comprehensive site visit reports and follow-up communications for investigators.

  • Contribute to study compliance by ensuring adherence to protocol requirements and reporting deviations appropriately.

Additional Responsibilities

  • Support the team with other study-related tasks as assigned, based on experience and training.

  • Maintain detailed documentation of site interactions, observations, and risk assessments to support centralized monitoring initiatives.

  • Collaborate with cross-functional teams including project management, data management, and medical monitoring to ensure seamless study execution.


Required Qualifications

Education

  • Bachelor’s degree in a field relevant to clinical research, nursing, or equivalent professional experience.

Experience

  • 1–3 years of on-site clinical monitoring experience in biotechnology, pharmaceutical, or CRO environments.

  • Demonstrated experience in dermatology clinical trials; exposure to rheumatology studies is a plus.

  • Experience with Phase 1 studies or units is an asset.

Skills & Competencies

  • Strong knowledge of ICH-GCP standards and regulatory requirements in Canada.

  • Fluent in English and French with excellent oral and written communication skills.

  • Proficient in Microsoft Office (Word, Excel, PowerPoint) and clinical trial data systems.

  • Ability to travel to research sites approximately 65% of the time.

  • Strong organizational skills, attention to detail, and the ability to prioritize multiple tasks under tight timelines.

  • Excellent judgment, problem-solving abilities, and ability to work independently or as part of a team.


Work Environment & Benefits

  • Flexible work schedule with the option to work remotely anywhere in Canada or from our 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.

  • Ongoing professional development and training opportunities in clinical research.

  • Collaborative and dynamic team environment emphasizing innovation, reliability, and responsiveness.


About Indero

Indero, formerly Innovaderm, is a global CRO specializing in dermatology and rheumatology. Since 2000, we have earned a reputation for excellence in clinical research and patient-focused service. Based in Montreal, we continue to grow across North America and Europe, delivering high-quality clinical trial solutions to biotech and pharmaceutical sponsors.

Indero is committed to equitable treatment and equal opportunity for all candidates. Accommodations are provided throughout the recruitment process for applicants with disabilities. Only candidates legally authorized to work in Canada will be considered.


Apply Now

Join Indero as a Bilingual CRA II and contribute to advancing dermatology and rheumatology clinical research while ensuring compliance, data quality, and patient safety across studies.