Senior Clinical Trial Manager – Boston, MA (M/F/X)

About Tissium

Tissium is a mission-driven medical device company founded in 2013, headquartered in Paris, with a production facility in Roncq (near Lille) and an office in Boston. We are dedicated to creating a new era of body repair by leveraging our biopolymer platform to develop innovative solutions in surgery for a positive impact on patients' lives.

Our technology is based on research and intellectual property from the laboratories of Professor Robert Langer (MIT) and Professor Jeffrey M. Karp (Brigham and Women's Hospital), who co-founded the company with Christophe Bancel (CEO) and Maria Pereira (Deputy CEO & Chief Innovation Officer).

We are developing polymers for atraumatic tissue repair in various applications. Today, these polymers are used for sutureless nerve repair, hernia repair, and cardiovascular sealing. Since our inception, we have raised a total of 170 million euros. Our latest fundraising round, which concluded in April 2023, resulted in 50 million euros in additional funding. This infusion of capital provides us with the necessary resources to finance the commercialization of our first products.

Responsibilities

• Independently manages clinical trials, including those conducted through Contract Research Organizations.
• Assumes overall responsibility for the development of protocols, clinical literature reviews, clinical trial reports, annual reports, risk/benefit analyses, informed consent templates, and other clinical documents.
• Develops study timelines, resource needs, and budgets and ensures accurate tracking and reporting of study metrics.
• Develops study plans including recruitment plan, monitoring plan, safety plan, other study-specific plans. Responsible for oversight of data management activities.
• Serves as primary contact for TISSIUM functional area representatives and vendors.
• Maintains regular communications with relevant departments such as R&D, Regulatory, Marketing, and others.
• Prepares and disseminates timely internal clinical trial updates.
• Responsible for the selection and day-to-day interaction with CROs and other external partners in the execution of assigned clinical trial(s). Monitors all outsourced activities including CROs, core laboratories and other external and internal partners.

Qualifications

• Bachelor's Degree in life sciences, health care or related discipline.
• 6+ years of Trial Management experience in MedTech (medical device), biotech, pharma, or a CRO.
• Working knowledge of Good Clinical Practice (GCP) and US and international regulations for clinical trials.
• Advanced written, oral, and interpersonal communication skills, including proficient knowledge of medical terminology.
• Systematic and efficient planning, decision making, prioritization, negotiation, and coordination skills.
• Thorough knowledge and record of compliance with relevant regulations including but not limited to GCP, ICH E6, 21 CFR, and other relevant regulations and guidances governing conduct of industry-sponsored clinical studies.

Tissium Behaviors & Mindset

• Act with a sense of urgency: Drive a culture of execution, accountability, and timely delivery aligned with critical milestones.
• Embrace calculated risk-taking: Make informed and thoughtful decisions that create positive cross-functional impact.
• Continuously learn and share: Foster a strong learning mindset, encourage knowledge sharing, and support team development.
• Challenge the status quo: Constructively question existing practices to improve systems, processes, and outcomes.
• Balance tactical and strategic thinking: Combine operational excellence with a clear mid-term vision and strategic priorities.
• Assume positive intent: Build trust and foster constructive, respectful, and psychologically safe collaboration across teams.
• Drive active collaboration: Coordinate multiple stakeholders effectively around shared objectives and business priorities.
• Own outcomes: Promote accountability and take responsibility for measurable project results and deliverables.
• Strive for excellence: Drive sustainable improvements in quality, compliance, operational performance, and continuous improvement.

Why Join Us

• A dynamic and stimulating environment, with a culture focused on initiative, learning, and continuous improvement.
• Real opportunities for growth and development, with evolving career paths and tailored training.
• The chance to join an ambitious startup at the forefront of high-impact medical innovation.
• A strong commitment to ESG, embedded in our strategy from day one.
• Athletic conditions: work-life balance, competitive package, and internal mobility (Paris, Roncq, Boston).
• An international and diverse environment, with more than 19 nationalities represented.

Hiring Process

• The journey starts with an interview with Talent Acquisition Manager (30 mins).
• Then a face-to-face (virtual) meeting with the Manager of the department you are applying to join (1 hour).
• This will then be followed by a Technical Interview to validate your practical job-related skills (1 hour).
• At the final stage, shortlisted candidates will be invited to a 90-minute team and culture fit interview, conducted either on-site or by videoconference.