Cambridge, Massachusetts, United States · On-site
DESCRIPTION OF THE COMPANY 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 creatin…
Skills: Clinical trial management, Site monitoring, Medical device support, Operating room support, ICH-GCP
Cambridge, Massachusetts, United States · Hybrid
$140k–$155k/yr
Description JOB TITLE: Senior Scientist, Analytical Science & Technology LOCATION: Cambridge, MA (hybrid-remote) REPORTS TO: Senior Manager, Analytical Science & Technology SALARY RANGE: $140,000 to $155,000 ABOUT THE PO…
Skills: Quality control, Method validation, Flow cytometry, cGMP, Analytical method lifecycle management
Cambridge, Massachusetts, United States · On-site
$126k–$171k/yr
Career CategoryOperationsJob DescriptionJoin Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious …
Skills: Analytical method development, Protein characterization, LC/MS, Peptide mapping, Disulfide mapping
Cambridge, Massachusetts, United States · On-site
$184k–$250k/yr
Career CategoryProcess DevelopmentJob Description Join Amgen’s Mission of Serving Patients At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living wit…
Skills: Bioprocess development, Cell culture, Downstream purification, Process characterization, Scale-up
Cambridge, Massachusetts, United States · On-site
Site: The Spaulding Rehabilitation Hospital Corporation Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance…
Skills: Plumbing Installation, System Maintenance, Blueprint Reading, Piping Diagrams, Massachusetts Plumbing Codes
BiogenCambridge, Massachusetts, United States · On-site
$117k–$157k/yr
About This Role: At Biogen, we are advancing science to deliver innovative therapies that transform patients’ lives. We are seeking a Scientist II to join our Analytical Development team as a Liquid Chromatography (LC) S…
Skills: Liquid chromatography, HPLC, UHPLC, LC-MS, Method development
Cambridge, Massachusetts, United States · On-site
About the Deliverome Project Deliverome Bio is a nonprofit startup building a first-of-its-kind open atlas of surface protein abundance and internalization. We’re hiring a founding team to generate the data that could ex…
Skills: Proteomics, Computational biology, LC-MS/MS, Spectronaut, Python
Cambridge, Massachusetts, United States · On-site
Who are we and why should you join us? ConcertAI is building the future of precision medicine. We use advanced artificial intelligence and real-world data to transform how healthcare and life sciences generate evidence, …
Skills: AWS, Terraform, CI/CD, Jenkins, GitHub Actions
Cambridge, Massachusetts, United States · On-site
$125k–$145k/yr
Description Scientist, Formulation Development At Merida Biosciences, we are pioneering true precision medicines for antibody-driven diseases. We specifically target pathogenic antibodies and their cellular sources with …
Skills: Formulation development, Biologics, Protein therapeutics, Stability studies, HPLC
Cambridge, Massachusetts, United States · On-site
$150k–$180k/yr
Blitzy is a Cambridge, MA based AI software development platform on a mission to revolutionize the software development life cycle by autonomously building custom software to unlock the next industrial revolution. We're …
Skills: Developer advocacy, Content creation, Technical writing, Public speaking, Software development
Cambridge, Massachusetts, United States · Remote OK
$105k–$168k/yr
Location: Remote, Northeast US Preference would be given to those based in Massachusetts Sartorius is looking for a strategic and results-driven Manager of Technical Sales Specialists to lead a high-performing team suppo…
Skills: Technical Sales, Pre-sales, Applications Consulting, CRM Proficiency, Consultative Selling
BiogenCambridge, Massachusetts, United States · Hybrid
$152k–$220k/yr
As Associate Director, Data Engineering & Architecture at Biogen, you will be an integral part of the Enterprise Application Services team, focusing on enhancing our data management and analytics capabilities. Reporting …
Skills: Data engineering, Data architecture, Snowflake, Data governance, Cloud data platforms
Cambridge, Massachusetts, United States · Remote OK
$121k–$219k/yr
Do you want to shape how AI models are validated, optimized, and deployed at global scale? Are you passionate about building the systems that ensure AI models perform reliably and responsibly in production Join the Akama…
Skills: Machine Learning, Python, PyTorch, TensorFlow, JAX
Relay TherapeuticsCambridge, Massachusetts, United States · On-site
$122k–$174k/yr
The Opportunity: You will be an integral part of Relay’s drug product development team supporting Relay's research and development programs. You will be responsible for design and development of pre-clinical formulations…
Skills: Pharmaceutics, Drug product development, Formulation development, Oral dosage forms, Pre-clinical research
Cambridge, Massachusetts, United States · Hybrid
$82k–$220k/yr
Overview: Draper is an independent, nonprofit research and development company headquartered in Cambridge, MA. The 2,000+ employees of Draper tackle important national challenges with a promise of delivering successful a…
Skills: Systems Engineering, Design Transfer, Manufacturing Readiness, Technical Program Management, Risk Management
Cambridge, Massachusetts, United States · On-site
$95k–$245k/yr
Overview: Draper is an independent, nonprofit research and development company headquartered in Cambridge, MA. The 2,000+ employees of Draper tackle important national challenges with a promise of delivering successful a…
Skills: Quality engineering, Lean Six Sigma, ISO 9001:2015, AS9100, Process integration
Cambridge, Massachusetts, United States · On-site
$20/hr–$45/hr
Overview: Draper is an independent, nonprofit research and development company headquartered in Cambridge, MA. The 2,000+ employees of Draper tackle important national challenges with a promise of delivering successful a…
Skills: C, C#, Python, Software development, Software testing
Cambridge, Massachusetts, United States · Hybrid
$63k–$101k/yr
The Role Immuno-Oncology Research at Moderna is seeking a talented and motivated Research Associate to join our efforts in developing new mRNA-based drugs for cancer therapy. The successful candidate will use molecular b…
Skills: Molecular biology, Immunology, Cell culture, Flow cytometry, ELISA
Cambridge, Massachusetts, United States · On-site
$95k–$245k/yr
Overview: Draper is an independent, nonprofit research and development company headquartered in Cambridge, MA. The 2,000+ employees of Draper tackle important national challenges with a promise of delivering successful a…
Skills: Software quality assurance, Model-based engineering, Algorithm design, Software testing, System architecture
Cambridge, Massachusetts, United States · Hybrid
$82k–$220k/yr
Overview: Draper is an independent, nonprofit research and development company headquartered in Cambridge, MA. The 2,000+ employees of Draper tackle important national challenges with a promise of delivering successful a…
Skills: System security, Cybersecurity architecture, Systems engineering, Hardware security, Software security
Cambridge, Massachusetts, United States • On-site
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The Field Clinical Product & Research Specialist is responsible for managing clinical trial sites, ensuring regulatory compliance, and performing field monitoring activities. Additionally, they provide on-site clinical and technical support to medical staff during procedures to ensure proper device utilization.
Candidates must hold an undergraduate degree in a relevant field such as Life Science, Nursing, or Biomedical Engineering. A minimum of 8 years of related experience is required, including at least 5 years in medical devices and field monitoring.
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.
The FCPRS is responsible for the successful execution of clinical trials by supporting site management and monitoring activities. Ensure assigned clinical studies comply with regulatory standards and protocols by conducting site visits, verifying data accuracy, and safeguarding patient rights. Typically works on studies with moderate to high complexity (in terms of design, location, regulatory requirements, etc.). Proactively identifies and resolves clinical site issues and participates in process improvement initiatives as required. Contributes to the development of clinical development plans, and other company initiatives as required. Additionally, FCPRS may be requested to support field-based clinical support by providing information and training to customers in the use of specific products in a clinical setting (e.g., operating room, outpatient clinic, etc.).
Responsible for site management and monitoring of assigned clinical study(ies). Collaborate with Study Management and other clinical operations staff to perform site management and field monitoring activities:
Establish and maintain excellent working relationships with external stakeholders such as Investigators, Study Coordinators and other site staff; and internal stakeholders to meet recruitment targets and to deliver high-quality data on time.
Ensure that all Adverse Events (AE), Serious Adverse Events (SAEs) and Product Quality Complaints are reported within the required reporting timelines and documented as appropriate.
Maintain and update trial management systems.
This individual will be required to perform field monitoring independently, including but not limited to qualifying site assessments, and initiation, interim and closeout visits.
Complete monitoring reports, follow-up letters etc. ensuring compliance to company SOPs and timelines.
Data monitoring activities, including on-site and remote review of study data for accuracy, integrity, and completeness
Build a collaborative partnership with CRAs and support as needed.
Assist the study team in planning clinical supplies and in particular, the Investigational Product. Ensuring that the product is available for the sites to support study enrollment.
Provide site training (Protocol, Amendment, GCP, etc.), as required.
Support the collection of essential documents and the maintenance of the TMF, as required.
Serves as the primary resource for clinical support in the areas of patient selection, basic troubleshooting, device utilization, and patient follow-up for company products.
Provide on-site clinical, technical, and educational support, guiding medical staff through use of commercially available medical devices, and troubleshooting products in operating rooms or other medical facilities.
Provides external staff training, and other product-related specifications, as requested.
Maintains a working knowledge of Company products, competitive devices, and new or competitive techniques used in surgery.
Performs other related duties as qualifications and training allows.
This role will report to the VP Clinicial Affairs.
You are to work independently and collaboratively within a team environment.
You have excellent interpersonal, time management, and oral and written communication skills.
You have strong written and oral communication skills and experience mentoring/coaching and providing training is preferred.
You are able to collaborate with all levels of management in a cross-functional team environment is required.
You love to travel to support customer and study meetings is a must (up to 60%); for domestic, trans-border and international.
At a minimum, completion of an undergraduate degree (e.g. Life Science, Nursing, Medicine, Biomedical Engineering, etc.) is required. Clinical Research Certification is an asset. Registered Nurse (RN certification) is a strong asset.
A minimum of 8+ years of related job experience is required for this position.
At least 5+ years of relevant experience within medical devices, surgery, and operating room support.
At least 5+ years of field monitoring and site management performing pre-study visits, initiation, interim, and close out visits.
Demonstrated working knowledge of ICH-GCP and FDA regulations.
Must have experience working with patients preferably in a clinical environment.
Proficient with MS Office and electronic databases (e.g., CTMS, IRT, eTMF).
Act with a sense of urgency: Align stakeholders around critical milestones and drive timely execution.
Embrace calculated risk-taking: Take thoughtful risks that create cross-functional impact.
Continuously learn and share: Demonstrate a strong learning mindset, share knowledge, and support team development.
Challenge the status quo: Question existing practices to improve systems, processes, and outcomes.
Balance tactical and strategic thinking: Combine operational excellence with a clear mid-term vision.
Assume positive intent: Foster constructive and respectful collaboration across teams.
Drive active collaboration: Coordinate multiple stakeholders toward shared objectives.
Own outcomes: Take responsibility for project results and deliverables.
Strive for excellence: Lead high-impact improvements in quality and performance.
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.
HR Interview (30 minutes)
Hiring Manager Interview (1 hour)
In some cases, we may also request professional references (including contact details).
Intrigued? We’d love to hear from you! Apply today - we’re standing by for your resume!
👉 We believe that building an inclusive company starts with a diverse team. We value diversity and encourage applications from people of all backgrounds. We are committed to equal opportunity and do not tolerate discrimination of any kind, including on the basis of gender, gender identity or expression, sexual orientation, origin, family situation, age, beliefs, disability, health status, or any other characteristic protected by law.
Our recruitment process is designed to be simple, transparent, and conversation-driven. We prioritize human interaction and ensure that every application is reviewed carefully and fairly.
Biomorphic Programmable Polymers
TISSIUM was founded in 2013 to address one of the most persistent medical challenges since the inception of surgical procedures: to reconstruct damaged tissue and restore its natural function. Since the discovery of our first polymer at the labs of Bob Langer and Jeff Karp at MIT, we recognized the exceptional potential for our technology to revolutionize the field of tissue reconstruction in multiple therapeutic areas. Our unique approach to product development leverages the knowledge gained from the development of our technology platform comprised of proprietary polymers, activation technologies, and delivery devices. We have developed a fully integrated innovation, design, commercialization and manufacturing platform to support our internal programs as well as co-development partnerships with leaders in the medtech industry.
Offices: 74, Rue du Faubourg Saint-Antoine, Paris, Ile-de-France 75012, FR · 2, rue Pierre-Antoine Delahousse, Parc Pierre Mauroy, Batiment B, Roncq, Hauts de France 59223, FR · 245 Main St, 2nd floor, Cambridge, Massachusetts 02142, US
Based on 627 listings with disclosed salaries, most engineering jobs in Cambridge, MA pay between $82k–$240k per year. Individual offers vary with seniority, company size, and specialization.
There are currently 786 open engineering positions in Cambridge, MA listed on Clera. New openings are added daily as companies post roles.
Companies currently hiring include Draper, Akamai Technologies, Lila Sciences, Flagship Pioneering, Harvard Division of Medical Sciences, among others. Browse the listings above to see every active employer.
Yes — 240 of the 786 open engineering positions offer remote or hybrid work (66 remote, 174 hybrid).
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