Sr. Clinical Study Manager

Arthrex•Pelican Bay, FL

About The Position

Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Arthrex is actively searching for a Sr. Clinical Study Manager. This individual will be responsible for leading and supporting clinical studies and projects aligned with Arthrex Research’s clinical research initiatives. The successful candidate will lead and oversee the full lifecycle of multicenter clinical studies, ensuring execution in compliance with research ethics, regulatory requirements, ISO standards, and internal procedures. This individual will drive study strategy, site management, monitoring activities, budgets, and cross-functional collaboration while serving as a key decision-maker for study operations, amendments, and risk management. The role also provides leadership and mentorship to research staff, ensuring the successful delivery of clinical research projects and portfolio objectives. Join our talented team at a global medical device company focused on Helping Surgeons Treat Their Patients Better™.

Requirements

Strong strategic thinking with the ability to translate goals into actionable project plans.
An understanding of cross-functional clinical study processes is required.
Ability to work in a team, good communication, documentation, and a strong understanding of data collection and analytical processes are required.
The ability to identify a research hypothesis and proposed outcome measures to address the hypothesis is required.
The ability to read a surgical technique and have a basic understanding of the instruments necessary to perform the procedure is required.
Able to communicate effectively with physicians, key opinion leaders, and other healthcare personnel.
Must have a strong understanding of federal regulations relating to clinical studies (FDA, MDR), ISO, and research ethics.
Proficiency in Microsoft Office programs
Clinical Research Certification required or must be willing to obtain within 1 year of employment.

Nice To Haves

Experience in managing research contracts and protocol development is preferred.
Experience in post-market, real world evidence, longitudinal or health economics studies is preferred.
Ability to generate and develop ideas that drive efficiency and impact organizational goals.
Ability to approach challenges with an innovative, solution-oriented mindset.
Bachelor’s degree required. Master’s degree preferred.
Three-year Sponsor/CRO preferred. Preferably, in a medical device industry environment
Familiarity with orthopedics and medical terminology is preferred.
Strong research and technical writing skills and ability to review protocols and agreements for accuracy.
Ability to organize and review data sets

Responsibilities

Leading, planning, executing, managing, and oversight of clinical studies according to research ethics guidelines, ISO standards, internal SOPs, applicable regulations, and portfolio priorities.
Leads the implementation of clinical protocols, informed consent forms, and study-related materials for clinical studies.
Manages site initiation activities (e.g., study start-up documentation preparation)
Responsible for IRB communication, including document preparation and submission of Arthrex study initiatives.
Implementing modifications to optimize protocol results or edit/amend study documentation if necessary.
Collaborate with Data Management team to ensure the electronic data capture system (EDC) is designed to collect all required data per the protocol.
Responsible for training internal staff assigned to studies.
Project lead for other research staff assigned to multicenter studies.
Key decision maker for study amendments and strategies
Maintain appropriate monitoring and maintenance of clinical sites to ensure the overall successful conduct of assigned clinical studies.
Oversee all aspects of the assigned clinical projects, including essential documents, electronic data collection, change management, risk management, and monitoring activities.
Set-up and maintain accurate progress and Site study status tracking logs to provide reports and updates of assigned clinical research projects.
Oversee follow-up and lead query resolution with sites via ongoing interactions.
Participation in investigator meetings, Site initiation, monitoring, and close-out visits when applicable
Complete central, remote, and on-site monitoring reports and follow-up letters
Complete monitoring report reviews of other staff
Oversee monitoring activities for the assigned projects and is responsible for ensuring actions are taken when applicable.
Identify and mitigate quality risk and/or issues associated with assigned studies/activities.
Facilitate appropriate documentation to maintain compliance with the Finance and Compliance departments.
Prepare and track clinical study budgets that include both sponsor costs and sites costs.
Responsible for the timely completion of deliverables, inclusive of contributing to interim and final study reports
Facilitate efficient utilization of available clinical data, addressing the needs of internal and external stakeholders (e.g., publications)
Works closely with leadership, product management, medical writing, project manager, and other research staff to manage assigned studies.
Conducts regular investigator meetings to ensure protocol compliance and site engagement.
Actively participate in research committees, study groups, and cross-functional portfolio governance activities to support continuous improvement and strategic alignment
Engage in and support departmental initiatives and cross-functional team projects, collaborating by driving execution, problem-solving, and achievement of key business outcomes.
Conducts project huddles and able to lead cross-functional projects.
Mentoring and training staff.
Serve as a cross-functional lead within an assigned study and product portfolio, ensuring alignment across Clinical Operations, Product Management, Data Management, Regulatory, Compliance, and other key stakeholders.