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Sr. Clinical Operations Lead

@ Alimentiv

Toronto, ON · London, ON

78k–130k $/anTélétravailTemps plein7+ ans d’expérience
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Alimentiv, a global clinical research organization focused on gastrointestinal disease therapies, is hiring a Senior Clinical Operations Lead to oversee regional or global clinical trials. The role leads Clinical Operations Leads and CRAs across monitoring, site management, and study start-up, and requires 7 to 9 years of clinical research experience (10+ preferred). Conditions stated include the full-time employment type and a monthly cell phone and remote work allowance dependent on role eligibility.

Salaire :

78 000 $–130 000 $ par année

Responsabilités :

  • Provide clinical operations oversight across assigned studies
  • Lead and mentor Clinical Operations Leads and CRAs
  • Oversee monitoring visits, recruitment, and essential documents
  • Lead country and site start-up and feasibility activities
  • Serve as liaison between monitoring, project management, and sponsors

Résumé des exigences :

  • 7 to 9 years of clinical research experience, 10+ preferred
  • Minimum 3 years hands-on CRA experience
  • Minimum 2 years clinical operations leadership
  • Strong knowledge of ICH-GCP and monitoring requirements
  • Experience with EDC systems and Microsoft Office

Outils et compétences

Source et dates

Site carrière / système de candidatures · lever

Date publiée par l’employeur
2026-06-05
Première détection par notre source
2026-11-06
Mise à jour du dossier source
2026-11-06

Ces dates décrivent le dossier source, pas une vérification en direct du recrutement. Consultez l’offre originale.

Détails du poste

NiveauSenior
DomaineProfessions paramédicales
Expérience7 an(s) et plus
Expérience en gestion2 an(s) et plus
Gestion d’équipeOui
Heures par semaine40 (estimé)
Milieu de travailBureau, Domicile
PositionSurtout assis
Exigences physiquesphysique faible · ordinateur élevé
LanguesEnglish
FormationBaccalauréat (préféré)
Avantages mentionnésCongés payés généreux, Horaire flexible, Aide aux études, Prime de rendement, Allocation de télétravail

Résumé et détails rédigés par l’IA à partir de l’offre; l’offre de l’employeur fait foi.

Alimentiv

Profil d’entreprise sauvegardé

Renseignements historiques provenant d’un profil The Jobs API sauvegardé (champs LinkedIn/Crunchbase). Ils ne sont pas vérifiés en temps réel; les chiffres peuvent avoir changé. Les valeurs manquantes restent inconnues.

Description complète de l’entreprise

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.

Abonnés LinkedIn
77 566
Personnes associées sur LinkedIn
645
Bureaux déclarés
  • 100 Dundas St, Suite 200, London, Ontario N6A 5B6, CA
  • 4350 Executive Dr, San Diego, US
  • Pietersbergweg 17, Amsterdam, NL
  • Suite 6, Level 2 29-31 Lexington Drive, Bella Vista , NSW 2153, AU
  • 150 King St W, Toronto, Ontario M5H 1J9, CA
Catégories d’activité
  • Health Care
  • Consulting
  • Clinical Trials
  • Biotechnology
  • Precision Medicine
  • Pharmaceutical
Autres noms enregistrés
  • Alimentiv
Spécialités
  • Medical Imaging
  • Medical Research & Development
  • Clinical Trial Services
  • Precision Medicine
  • Biomarker Discovery
  • Histopathology
  • Biostatistics
  • Real-World Evidence
  • Phase 1-4 Clinical Trials
  • IBD
  • EGID/EoE
  • Celiac Disease
  • and Ulcerative Colitis
Le profil indique une agence de recrutement
Non
Investissement total déclaré
0

La devise et la date d’observation ne sont pas fournies; ce n’est ni une valorisation actuelle ni une ronde de financement.

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…

ChampValeur
SecteurPharmaceutical Manufacturing
Taille501-1,000 employees
Siège socialLondon, Ontario
Type d’organisationPrivately Held
Fondée en1986
SpécialitésMedical ImagingMedical Research & DevelopmentClinical Trial ServicesPrecision MedicineBiomarker DiscoveryHistopathologyBiostatisticsReal-World EvidencePhase 1-4 Clinical TrialsIBD
Offres sur Jobsy11
LinkedInVoir la page
Description

Alimentiv is a global CRO with a singular focus: advancing therapies for patients with gastrointestinal diseases. GI is our WHY and for more than 30 years that purpose has driven our scientific rigour, operational excellence, and deep therapeutic expertise, including supporting more than 70% of IBD compounds in development.
We operate as a private, profit-with-purpose company, channeling our commercial success back into scientific research, technology, and our people. With approximately 700 people across multiple countries and three service lines, we are growing deliberately, and the capability of our leaders and our organization is central to how we get there.

If you want to do meaningful work, build something real, and invest back in research that changes lives — we want to meet you!

Job Overview

The Senior Clinical Operations Lead (Sr COL) provides clinical operations leadership and oversight for regional and global clinical trials, ensuring high-quality delivery across monitoring and site management activities.

Working closely with Clinical Project Management, Clinical Operations Leads (COLs), Clinical Research Associates (CRAs), investigative sites and cross-functional teams, the Sr COL is responsible for ensuring study activities are delivered in accordance with the protocol, Monitoring Plan, ICH-GCP, applicable regulations and project timelines.

This role provides operational leadership across the study lifecycle, including country and site start-up, monitoring oversight, enrolment and recruitment, CRA/COL guidance and training, study documentation, performance metrics, issue escalation and corrective actions. The Sr COL may also represent Monitoring & Site Management in Sponsor meetings and provide broader trial management support as required.

Key Responsabilities

  • Provide regional and/or global clinical operations oversight across assigned studies, ensuring compliance with study protocols, Monitoring Plans, ICH-GCP, applicable regulations and project timelines.

  • Lead and oversee Clinical Operations Leads (COLs) and CRAs, providing study-specific guidance, training, mentoring and operational support throughout the project lifecycle.

  • Oversee key monitoring and site management deliverables, including monitoring visit schedules and reports, recruitment progress, essential document collection, protocol deviations and compliance with the Monitoring Plan.

  • Lead and support country and site feasibility, selection and start-up activities, providing Monitoring & Site Management input into country and site strategies.

  • Serve as a key liaison between the monitoring team, Clinical Project Management, cross-functional study teams and Sponsors, escalating risks and issues and supporting appropriate corrective actions.

  • Develop and maintain study-specific operational documentation and tools, including Monitoring Plans, CRA/site training materials, study tools and enrolment and recruitment strategies.

  • Review monitoring visit reports and study performance metrics to ensure quality, consistency, appropriate site management and timely delivery.

  • Lead CRA/COL meetings and represent Monitoring & Site Management during Sponsor meetings, study kick-offs, Investigator Meetings and other project discussions as required.

  • Support project and monitoring budget oversight, including monitoring resource planning, visit forecasts, site payments, pass-through expenses and other project financial activities as applicable.

  • Contribute to departmental and company initiatives, support business development and Sponsor activities where required, and provide mentorship to COLs and other clinical operations colleagues.

Skills & Qualifications

Approximately 7–9 years of relevant clinical research experience; 10+ years is preferred.

  • Minimum of 3 years of hands-on CRA experience and 2 years of Clinical Operations Lead (COL) or equivalent clinical operations leadership experience.

  • Bachelor’s degree in a relevant discipline preferred; an equivalent combination of education and relevant clinical research experience may be considered.

  • Strong knowledge of ICH-GCP, clinical monitoring requirements, IRB/EC processes, Investigator responsibilities and applicable local regulations.

  • Demonstrated experience providing operational oversight across clinical studies, including monitoring, site management, study start-up and study-level deliverables.

  • Strong experience reviewing monitoring reports, clinical research documentation, protocol deviations, study metrics and operational risks.

  • Experience working with EDC systems and proficiency with Microsoft Office applications.

  • Strong written and verbal communication skills with the ability to work effectively with CRAs, COLs, project teams, Sponsors and other cross-functional stakeholders.

  • Highly organised and proactive, with strong attention to detail and the ability to prioritise multiple deliverables and meet deadlines in a dynamic environment.

  • Strong leadership, mentoring, problem-solving and interpersonal skills, with the ability to provide guidance and influence stakeholders without formal direct-line authority.

  • What We Offer

      In addition, as an Alimentiv Employee, you’re also eligible for the following programs:

      • Education Reimbursement program for full-time employees
      • Monthly Cell Phone and Remote Work Allowance (dependent on role eligibility)
      • One time office setup allowance (can be used to purchase a scanner/printer, extra monitor, office furniture, etc.)
      • Working while visiting program – up to 4 weeks per year!
      • Flexible Summer Hours Program from May – September
      • Employee referral incentive – we know great people know other great people, and we think that warrants recognition!
      • Full-time employees also become beneficiaries of the Alimentiv Trust after one year of employment, and permanent members after 5 years of employment
      • Optional formal mentorship program (Alimentorship); country/region annual social events in person; leadership development programs for people leaders in accordance with your seniority; social committee and several other optional initiatives designed to support you in feeling like part of the Alimentiv team!
      • Additional benefits may be available depending on the country of employment and are subject to local policies and eligibility.

    Our Services

    • End-to-end GI clinical trial services, from protocol design through submission support
    • Central medical imaging management and endoscopic reading
    • Precision medicine and biomarker solutions
    • Real-world evidence and clinical consulting
    • Histopathology and lab services through AcelaBio

    How to Apply

      To apply for this position, please submit your resume through the Alimentiv Careers Portal or via LinkedIn’s Easy Apply. Resumes must be submitted in English.

    Equal Opportunity and Accessibility

      Alimentiv is committed to building a diverse, inclusive and respectful workplace. We are an equal opportunity employer and consider all qualified applicants for employment without regard to race, colour, ethnicity, national origin, religion or belief, sex, gender identity or expression, sexual orientation, age, marital or family status, disability, or any other characteristic protected by applicable law.

      Accommodations are available upon request for persons with disabilities throughout the recruitment and selection process. Requests can be directed to [email protected].

    Stay Alert to Recruitment Scams

    Alimentiv is aware of a continued increase in phishing scams, which use various methods of attack via email, text, voice and social media, including individuals posing as our recruiters and contacting candidates with fraudulent opportunities. Our hiring process always includes direct engagement with a recruiter or hiring manager, and we will never ask for sensitive personal information early in the process.

    Official communication will only come from company email addresses containing "@alimentiv.com". If you are contacted about an open job at Alimentiv, please verify the domain of the sender's email address and confirm that you are being asked to apply on this website. If something doesn't feel right, we encourage you to verify before responding. If you believe you have been the victim of a phishing scam, please contact your local government cyber authority to report it.

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