Clinical Scientist/Scientifique clinique, Canada

Indero (formerly Innovaderm); Toronto; Remote; CAD 80,000 - 100,000; Full time

Job summary

A leading contract research organization is seeking a Clinical Scientist to handle medical writing activities. The ideal candidate will produce high-quality scientific documents and collaborate on clinical studies. This position offers flexible working options and a supportive environment focused on innovation and collaboration.

Benefits

Flexible work schedule

Complete benefits (RRSP, medical, dental, vision, etc.)

Ongoing learning and development

Qualifications

• Experience in writing clinical/regulatory documents.
• Good knowledge of good clinical practices.

Responsibilities

• Accountable for medical writing deliverables and quality.
• Collaborates on clinical development of various studies.
• Contributes to study design and writes clinical protocols.

Skills

Medical Writing

Attention to Detail

English Communication

Adaptability

Education

MSc in Life Sciences

PhD

Tools

Word

Job description

The Clinical Scientist is responsible for medical writing activities at Indero. The individual will author or contribute to development of clinical and regulatory documents (synopsis, study protocols, statistical analysis plans, clinical study reports), as well as scientific publications.

This role will be perfect for you if:

• You are a strong medical writer with demonstrated ability to produce high-quality scientific documents to support clinical research.
• You enjoy learning continuously and keeping yourself informed.
• Having an impact within a growing company with momentum motivates you.

Responsibilities:

• Accountable for own medical writing deliverables, including quality, stakeholder communication, resolution of project issues, and timeline management;
• Collaborates on clinical development of Phase 1/First-in-Man studies, Proof of Concept (POC) trials, Phase 2b – 3 studies, and Phase 4/registry trials.
• Contributes to study design and writes/reviews clinical study protocols/amendments;
• Reviews informed consent/assent forms, study reference manuals, statistical analysis plans, and mock shells of statistical tables/figures/listings;
• Reviews, analyzes, and interprets study data based on scientific expertise and industry standards;
• Writes/reviews narratives and clinical study reports;
• Prepares scientific abstracts, posters, and manuscripts;
• Performs online literature searches;
• Provides documents with high quality in terms of scientific content, organization, clarity, accuracy, format, and consistency;
• May perform quality control review of documents prepared by other team members;
• Participates in process improvement efforts of the department.

Requirements:

IDEAL PROFILE

• MSc in life sciences; PhD is an asset;

Experience

• Experience in writing clinical/regulatory documents such as study protocols and clinical study reports;
• Experience analyzing and reporting on study data

Knowledge And Skills

• Good knowledge of good clinical practices, and applicable Health Canada and FDA regulations/guidelines.
• Good knowledge of drug development process;
• Advanced English writing skills; strong English communication skills; French is an asset;
• Strong proficiency in Word;
• Ability to handle varied and multiple tasks, organize own work, and prioritize workload;
• Excellent attention to detail;
• Client-focused attitude;
• Quick learner, good adaptability, and versatility.

Our company:

The work environment

At Indero, you will work with brilliant and driven colleagues. Our values are collaboration, innovation, reliability, and responsiveness. We offer a stimulating work environment and attractive advancement opportunities.

In this position, you will be eligible for the following perks:

• Flexible work schedule
• Full-time permanent position
• Complete benefits (RRSP, medical, dental, vision, vacation, personal days, virtual medical clinic, social activities)
• Ongoing learning and development

Work location

The successful candidate for this position is given the option to work from home anywhere in Canada, or from our headquarters in Montreal (in accordance with company policies and public health directives).

Occasional visits to our Montreal headquarters may be required or encouraged.

About Indero

Indero is a contract research organization (CRO) specialized in dermatology and rheumatology. Since its beginnings in 2000, our organization has benefited from a solid reputation for the quality of its research and services exceeding the expectations of its clients. Based in Montreal, Indero continues to grow and expand in North America and Europe.

Indero is committed to providing equitable treatment and equal opportunity to all individuals. As such, Indero will provide accommodations throughout the recruitment and selection process to applicants with disabilities, upon request.