Clinical Content Specialist, Regulatory Documents

Job Title: Clinical Content SpecialistWe are seeking an experienced and detail-oriented Clinical Content Specialist to join our team at Pharma Medica Research Inc.About Us:Pharma Medica Research Inc. is a Contract Research Organization dedicated to delivering high-quality clinical trials services in a highly regulated industry.Estimated Salary Range: $80,000...

Job SummaryWe are seeking a highly skilled Clinical Documentation Specialist to join our team at Pharma Medica Research Inc.About UsPharma Medica Research Inc. is a Contract Research Organization that specializes in conducting early phase clinical trials. We are committed to innovation and original solutions in a highly regulated industry.Key...

**About Pharma Medica Research Inc.**We are a Contract Research Organization specializing in early phase clinical trials, seeking an experienced Senior Clinical Content Developer. Located in Mississauga, we strive for innovation and excellence in the highly regulated pharmaceutical industry.Key Responsibilities:Develop high-quality study-related materials...

OverviewPharma Medica Research Inc. is a contract research organization that strives for innovation and original solutions in a highly regulated industry.Estimated Salary: $85,000 - $110,000 per yearJob DescriptionWe are currently seeking a skilled Clinical Documentation Specialist to join our team in Mississauga. As a key member of our team, you will be...

Job Description:The Senior Scientific Communications Specialist is a professional with in-depth knowledge of scientific, clinical, and therapeutic area expertise. This role is responsible for overseeing staff and client services, providing scientifically accurate and balanced information to internal stakeholders, external healthcare professionals, and...

Job DescriptionWe are seeking an experienced Regulatory Medical Writer to join our team at GSK.The ideal candidate will have a strong background in clinical trial design, research data analysis, and regulatory document writing.About the RoleThis is a senior-level position that requires advanced expertise in clinical document writing, including protocols,...

Job Title:Pharmaceutical Communications SpecialistJob Description:Job Summary:The Pharmaceutical Communications Specialist will oversee staff and client services with scientific, clinical, and therapeutic area expertise. Key responsibilities include creating scientifically accurate and balanced information for internal stakeholders, external healthcare...

Unlock Your Potential in Regulatory DataAt Roche, we're committed to fostering diversity, equity, and inclusion in our pursuit of exceptional care. As a key member of our Pharma Development Regulatory team, you'll play a vital role in driving our mission forward.The Opportunity:Assist in the preparation of regulatory content, ensuring alignment with...

About Pharma Medica Research Inc.">Pharma Medica Research Inc. is a Contract Research Organization that strives for innovation and original solutions in a highly regulated industry. We are a full service contract research organization specialized in conducting early phase clinical trials in healthy volunteers, special populations and patient groups. Our team...

Job SummaryWe are seeking a highly skilled Regulatory Compliance Specialist to join our team at PointClickCare. This role will play a crucial part in driving key initiatives and projects that have a significant impact on our company, customers, and stakeholders.In this capacity, you will work closely with colleagues from various departments, including...

We are seeking a highly skilled Content Creator to join our team at the i3 Institute. This is a temporary, full-time position with 40 hours of work per week.Job SummaryThis role involves creating high-quality technical documentation, user guides, and other written materials to explain complex software, electronic, mechanical, and equipment installations,...

About Pharma Medica Research Inc.We are a Contract Research Organization that strives for innovation and original solutions in the highly regulated and competitive pharmaceutical industry.Job Title: Associate Medical Writer, RegulatoryCompensation Package:The estimated annual salary range for this position is $80,000 to $120,000 CAD, depending on...

At Brenntag Specialities, we are seeking a highly skilled Regulatory Affairs Specialist to join our team in Mississauga. This role is responsible for providing support to the organization in maintaining compliance and addressing needs related to new and existing business as they pertain to regulatory matters.Key ResponsibilitiesManage risk considering legal...

About Pharma Medica Research Inc.Pharma Medica Research (PMRI) is a Contract Research Organization that strives for innovation and original solutions in a highly regulated industry. We are a full-service contract research organization specializing in conducting early-phase clinical trials in healthy volunteers, special populations, and patient groups.Our...

About Pharma Medica Research Inc.We are a full-service contract research organization specializing in early-phase clinical trials for healthy volunteers, special populations, and patients.Our team is seeking a Bioanalytical Specialist to join our bioanalytical laboratory.Job DescriptionThe Bioanalytical Specialist will perform various tasks to support...

We are seeking an experienced Content Creation Specialist to join our team at Search Gurus Inc.The ideal candidate will have 2 years of experience in content creation, with a strong portfolio that showcases their writing skills and ability to work independently.As a Content Creation Specialist, you will be responsible for creating high-quality content that...

Brenntag Specialties is committed to building a workforce that reflects the communities we serve and to promote a diverse, inclusive, accessible, merit-based, respectful and equitable workplace.Role OverviewThe Regulatory Compliance Specialist will provide support to the organization in maintaining compliance and addressing needs related to new and existing...

About the Rolei3 Institute is seeking a skilled Content Creator and Digital Specialist to join our team. As a key member of our organization, you will be responsible for creating engaging content that showcases our mission and values.Key ResponsibilitiesAnalyze material, write manuals, user guides, and other documents to explain clearly and concisely the...

We are seeking a highly skilled Regulatory Compliance Specialist to join our team in Mississauga. As a key member of our Regulatory Affairs department, you will play a critical role in ensuring the company's compliance with Canadian chemical control and environmental regulations.Job SummaryThis is an exciting opportunity for a professional with a strong...

About UsThe Electrical Safety Authority is a government-mandated organization responsible for improving electrical safety in Ontario. Our mission is to anticipate, understand, and prevent electrical-related harms.Job Title: Electrical Safety Content SpecialistWe are seeking an experienced content specialist to join our team. This role involves researching,...