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Project Management

At Seriant, we do more than just manage your trial; we own it, lead it, and advocate for you at every step.

 

We make sure your trial is in expert hands so you can focus on bringing life-changing treatments to patients.

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Our project managers ensure your study moves forward efficiently while maintaining the highest standards of data integrity, patient safety, and compliance. With a relentless focus on speed, precision, tight control over every part of the project lifecycle.

We are an Agile Local Team with a global reach. With a core team based in Montreal, we make quick decisions and ensure fast turnaround times, keeping your study moving forward.

  • Hands-On Leadership— Our project managers oversee every aspect of your study, from contract and budget negotiations to feasibility, site activation, recruitment, and study closeout, ensuring accountability and consistency
  • Global Reach, Local Expertise— Our trusted global network provides in-country regulatory and operational expertise to navigate regional complexities seamlessly
  • Relationships & Engagement Matter— We prioritize strong collaboration with sites, sponsors, and vendors, fostering trust and alignment to ensure trial success
  • Cutting-Edge Technology & Decentralized Solutions— We leverage the latest clinical trial technologies to streamline operations and enhance patient and site engagement
  • Robust Vendor Management— We take a strategic, proactive approach to managing vendors, ensuring high-quality, cost-effective execution across all study phases

We provide expert guidance from study inception through execution, leveraging data-driven insights, advanced solutions, and seamless coordination to optimize trial success.

  • Study Design & Initial Strategy
  • Embedded Regulatory & Biostatistics Expertise— Ensuring study design aligns with submission expectations from day one
  • Recommendations on countries, sites, and technologies to enhance trial outcomes
  • Recruitment Forecasting, Modelling & Benchmarking
  • Recruitment and Engagement Strategies

We ensure seamless trial execution through data-driven oversight, proactive risk management, and agile adaptability, optimizing performance at every stage of the study.

  • Data-Driven Decision Making & controls over the entire project lifecycle via metrics and signals of project health
  • Data Driven Oversight via Reports, dashboards and modeling for better forecasting and efficiency
  • Key Performance Metrics— Leveraging analytics to track progress, identify bottlenecks, and optimize decision-making in every phase of your study from startup to recruitment to closeout
  • Driving Critical Data Deliveries & key study milestones
  • Strong Risk Management embedded in everything we do, every day

We create a fully integrated team, uniting sponsors, vendors, and site staff while seamlessly connecting regulatory, clinical, and operational functions to ensure agility and alignment with study goals.

  • Ensuring that ALL members of the team, including vendors, sponsor teams, and site staff are united as one team towards each study’s goals
  • Integrate project management, regulatory compliance, clinical operations, and biostatistics to ensure optimal execution and adherence to various requirements
  • Adapting quickly to study changes, protocol amendments, and change management

We prioritize patients and sites by providing tailored support, streamlined recruitment strategies, and proactive engagement to enhance compliance, retention, and study success.

  • Personalized Site Support & training
  • Patient-First Approach— Designing studies with the patient experience in mind, leading to higher compliance and participation rates
  • Recruitment strategies to minimize site burden and improve recruitment/retention rates
  • Communication plans ensure that site and patient engagement is high, to building & maintain a team that goes above and beyond

Interested in this service?
Let’s work together!

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