Alimentiv

4 Jobs

597 Employees

About the Company

Industry-leading specialty GI contract research organization (CRO) transforming clinical trial outcomes and accelerating the development of life-changing therapies. We bring together deep GI expertise, advanced medical imaging solutions, clinical operation excellence and cutting-edge precision medicine/laboratory services.

With a global network of 5,000+ sites in >60 countries and growing, we expedite study activation and maximize patient enrollment, ensuring efficient and impactful clinical trials. Trusted by pharmaceutical and biotech partners, we support over 70% of all IBD compounds in development today - delivering customized end-to-end solutions to bring novel therapies to market.

As a full-service CRO, our offering is tailored to meet your specific clinical research needs:
* Clinical Trial Services
* Medical Monitoring
* Medical Imaging Solutions
* Medical Research & Development
* Medical Writing
* Precision Medicine/Biomarkers
* Clinical Pharmacology
* Histopathology via Specialty Lab, AcelaBio
* Spatial Biology
* Statistics
* Real-World Evidence

Headquartered in London, Ontario, Alimentiv operates with globally across Canada, the US, Europe, Asia-Pacific, and Latin America.

Listed Jobs

Company Name: Alimentiv
Job Title: Senior Content Marketing Specialist
Job Description: **Job Title:** Senior Content Marketing Specialist **Role Summary:** Leads the creation, execution, and measurement of integrated marketing communications to boost brand visibility, lead generation, and audience engagement for a life‑sciences organization. Manages content development across digital, print, and event channels, collaborates with cross‑functional teams and external partners, and ensures all messaging aligns with brand standards and strategic goals. **Expectations:** - Deliver high‑quality, technically accurate content for B2B audiences. - Drive end‑to‑end campaign management from concept through performance analysis. - Maintain consistency of brand voice across all channels and assets. - Optimize content for SEO and marketing automation to support demand generation. - Manage budgets, vendor relationships, and documentation with minimal supervision. **Key Responsibilities:** - Create and edit copy for brochures, blogs, emails, ads, videos, press releases, and presentations. - Develop and maintain social media calendars; write and schedule posts for LinkedIn, X, etc. - Partner with graphic designers to align visuals with messaging. - Lead project management of marketing assets, including interviews, approvals, and archiving. - Produce website and landing‑page content; ensure SEO best practices with Digital Marketing Manager. - Write copy for lead‑generation and automated nurture campaigns; collaborate with Inside Sales. - Design promotional content and advertising plans for conferences, webinars, and roadshows; coordinate with event vendors. - Track campaign expenses, maintain budget reports, and update project dashboards. - Evaluate and recommend new content vendors/ agencies; maintain collateral inventory and archives. - Provide consultative guidance to stakeholders on messaging and delivery methods. **Required Skills:** - Strong written and verbal communication; meticulous attention to detail. - Ability to translate complex scientific/technical information into clear marketing copy. - B2B marketing expertise, preferably in Clinical Research, CRO, Pharmaceutical, or Life Sciences. - Proficiency with marketing automation platforms (e.g., HubSpot). - Social media fluency for organic and paid campaigns (LinkedIn, X, Instagram). - Project‑management tools experience (Monday.com, Asana, Smartsheet). - SEO knowledge and content optimization. - Analytical skills for dashboarding, metrics, and campaign performance reporting. - Vendor and stakeholder management; consultative approach. **Required Education & Certifications:** - Minimum 4–6 years of relevant marketing/communications experience. - Bachelor’s degree (or equivalent) in Marketing, Communications, Business, or a related field; certificate/diploma accepted. - Preference for candidates with global CRO experience and EST‑time‑zone alignment.

Company Name: Alimentiv
Job Title: Product Support Specialist
Job Description: **Job Title:** Product Support Specialist **Role Summary:** Acts as a technical liaison between customers and product teams to resolve issues, improve product performance, and enhance user experience for medical imaging hardware and software in clinical trials. **Expectations:** Tier one technical support, issue triage and escalation, cross-functional collaboration, knowledge base management, and support for reporting and process improvement initiatives. **Key Responsibilities:** - Prioritize, diagnose, troubleshoot, categorize, and escalate technical issues related to medical imaging hardware and software. - Maintain and update knowledge base documentation, troubleshooting guides, and support resources. - Collaborate with Service Desk, project management, product development, and IT teams to resolve customer requests. - Track and analyze support metrics, generate reports on resolution times, customer satisfaction, and recurring issues. - Contribute to product improvement by identifying trends, reviewing test cases, and providing feedback from user support data. - Support requests for technical information on product specifications and functionality. **Required Skills:** - Problem-solving, analytical skills, and technical troubleshooting expertise for hardware/software compatibility and bugs. - Proficiency in helpdesk/ticketing systems (e.g., Service Now) and ITSM tools. - Experience with JIRA, GitHub Issues, or similar project/defect management platforms. - Strong written/verbal communication with a customer-focused approach. - Ability to handle repetitive tasks, prolonged standing, and physical lifting (25–50 lbs) for hardware testing. **Required Education & Certifications:** - Associates degree or diploma in Computer Science, Engineering, or relevant field; bachelor’s degree preferred. - 1–3 years in IT technical support or equivalent role (optional but advantageous).

Company Name: Alimentiv
Job Title: Sr. Statistician
Job Description: Job title: Sr. Statistician Role Summary: Lead biostatistical operations in clinical research, overseeing statistical planning, analysis, reporting, and team management. Expectations: Deliver rigorous, compliant statistical solutions across study life cycles; drive methodological excellence and mentor SAS programmers. Key Responsibilities - Develop and execute statistical analysis plans, including sample size, randomization, and hypothesis testing. - Perform and interpret statistical analyses using standard software (e.g., SAS), translating results for clinical and regulatory reports. - Guide study teams on protocols, data capture, and analysis methodology; ensure alignment with regulatory and organizational standards. - Lead post‑study reporting: statistical sections of study reports, publications, and presentations. - Manage and develop a team of statisticians and SAS programmers: assign studies, evaluate performance, coach, and provide training. - Collaborate with data management, medical writing, and external stakeholders to ensure data integrity and scientific quality. Required Skills - Advanced statistical methodology knowledge and experience in clinical trials. - Proficiency in SAS and statistical software. - Strong leadership and people‑management abilities. - Excellent written and verbal communication, and the ability to translate complex data into clear scientific narratives. Required Education & Certifications - Minimum: Bachelor’s degree in Statistics, Biostatistics, or related field plus professional certifications. - Preferred: Master’s or Ph.D. in Statistics/Biostatistics with research or industry experience. - Regulatory and clinical trials experience is a plus.

Company Name: Alimentiv
Job Title: Consulting Statistician
Job Description: **Job Title:** Consulting Statistician **Role Summary:** Drive the development and application of biostatistical methods for clinical studies, advising clients on study design, analysis, and interpretation. Lead preparation of statistical analysis plans, ensure regulatory compliance, and communicate complex concepts to non‑statistical stakeholders. Engage in thought leadership, business development, and continuous learning to advance the Statistical Center of Excellence. **Expectations:** - Deliver high‑quality, evidence‑based statistical guidance for clinical trials. - Translate scientific questions into robust statistical hypotheses and designs. - Communicate findings clearly to cross‑functional teams and external clients. - Contribute to professional growth and business development through presentations, publications, and proposal support. **Key Responsibilities:** - Create and review statistical analysis plans, study protocols, and reporting documents. - Advise on study design, sample size, randomization, and data collection strategies. - Evaluate and recommend innovative statistical methods aligned with regulatory standards. - Collaborate with project teams to ensure data integrity, appropriate analysis, and compliance. - Prepare statistical sections for clinical study reports, publications, and presentations. - Deliver training and educational materials to clients and internal stakeholders. - Represent the organization at conferences, contribute to scientific content, and produce white papers or case studies. - Support business development by developing proposal content, participating in bid defenses, and presenting statistical concepts to prospective clients. - Monitor emerging research and regulatory updates in biostatistics and therapy‑specific areas. **Required Skills:** - Advanced knowledge of biostatistical methodologies and regulatory requirements (FDA/EMA). - Proficiency in statistical software (R, SAS, Stata, or similar). - Strong analytical, problem‑solving, and critical thinking abilities. - Exceptional oral and written communication, with ability to simplify complex concepts. - Experience in preparing statistical analysis plans and regulatory documentation. - Project management skills and ability to work collaboratively with multidisciplinary teams. - Ability to develop educational and business development materials. **Required Education & Certifications:** - Master’s degree in Statistics, Biostatistics, Epidemiology, or related quantitative science. - Minimum 4–6 years of professional experience in clinical trial statistics or biostatistics. - Advanced degrees (Ph.D., DO, or equivalent) and specialist certifications (e.g., ASA, ASA‑MS) are considered assets.