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

Tissium
Cambridge, MA

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Job Details

Benefits

Internal mobility program

Qualifications

Project team coordination
Project reporting
Research project management
Research design
Clinical study protocols and reports
6 years
Regulatory documents
Informed consent
Clinical trial risk management
Metrics Reporting
Critical literature reviews
Schedule management
ICH guidelines
Bachelor's degree
Budget planning
Data management
Continuous improvement
Decision making
Content development
Clinical data report preparation
Vendor relationship management
Contingency planning
Vendor communication
Relationship management
Patient recruitment
Managing medical device development budgets
Project resource management
Clinical quality assurance standards
Senior level
Clinical research reports

Full Job Description

COMPANY DESCRIPTION

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.

Tissium’s 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

The Senior Clinical Trial Manager (Boston-based) will assume responsibility for the planning and execution of clinical trials. This individual will be responsible for study timelines and budgets, preparation of study-related materials, relationship management between study sites and CROs, supervision of study activities, identification of project risks, and contingency planning.

The position is based in Boston, Massachusetts, and will play a key role in the successful delivery of Tissium's clinical development programs.

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.
Coordinates the design, format and content of study guides and subject instructions; participates in the development of Investigator Brochures.
Serve as primary contact for TISSIUM functional area representatives and vendors.
Maintains regular communications with relevant departments such as R&D, Regulatory, Marketing, and others.
Prepare and disseminate 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.

YOUR BACKGROUND

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.
Attractive 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.

Intrigued? We’d love to hear from you! Apply today - we’re standing by for your resume!

We firmly believe that building a company for everyone requires a diverse team. Our organisation values diversity and welcomes applications from individuals of all backgrounds. We do not discriminate against employees or applicants based on gender identity or expression, sexual orientation, race, religion, age, national origin, citizenship, disability, pregnancy status, veteran status, or any other differences. Our company culture prioritises human interaction and ensures that every individual's voice is heard, making our processes lightweight yet efficient.

Apply Now

Refine Your Search

trial manager m jobs

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

Manager - Engineering

Legal Records Manager

Litigation Attorney - Family Law

Manager - Process Development, Downstream

Engineer – Engineering

Claims Manager

Litigation Attorney

R&D Lab Technician

Injection Process Engineer

Clinical Program Scheduler & Office Admin

Senior Manager, Clinical Guidelines

Clinical Research Site Operation Leader

Controller

Accounting Manager

Quality Assurance Supervisor

LEAD ENGINEER II RD

Product line specialist

Paid Media Associate

REMOTE Auto Subrogation Attorney – California Bar Required!

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