Role Description
We are searching for the best talent for a Senior Manager, Clinical R&D β Joints Robotics to join our Orthopaedics team. This is a remote position, but our ideal candidate will be based in Boston, MA or Warsaw, IN. There may be travel required up to 20%.
Purpose:
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Lead clinical research and development for joint robotics products across the DePuy Synthes portfolio.
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Own clinical strategy, clinical inputs to R&D, complaints handling investigations, execution oversight, data interpretation, and external scientific communication to support product development, regulatory submissions, and adoption by surgeons and health systems.
Key Responsibilities:
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Define and execute clinical R&D strategy for joints robotics (pre-market inputs and post-market rolls outs and investigations).
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Collaborate cross-functionally with engineering, regulatory, quality, clinical affairs, marketing, and commercial to align clinical plans with product and regulatory objectives.
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Assist in gathering voice of customers from the field and potential future users.
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Help distil clinical and commercial inputs towards new product development.
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Lead the clinical field investigations pipeline and execution.
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Lead the new product roll out R&D support to the field and R&D support to train the trainers.
Qualifications
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Bachelorβs degree in Engineering or equivalent technical degree OR surgical Medical degree equivalent.
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4+ years of relevant experience in medical surgical field and/or device clinical research, R&D, or clinical operations.
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Surgical/clinical exposure (OR observation or engagement with high-volume surgeons).
Requirements
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7+ years of relevant experience in medical device clinical research, R&D, or clinical operations, with proven experience supporting product development (manufacturing or pure clinical roles OK if demonstrated cross-functional impact).
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Demonstrated ability to work with cross-functional teams and external clinical partners.
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Prior direct experience in orthopedics, joint replacement, or surgical robotics.
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Working knowledge of regulatory pathways (FDA, EU MDR, other regional regulators) and clinical compliance (GCP).
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Strong project management skills; experience with budgeting and resource forecasting.
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Strategic thinker with hands-on execution ability.
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Influential communicator and collaborator across technical and clinical stakeholders.
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Patient outcomes focused.
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Ability to lead and grow a high-performing team.
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Strong written and verbal communication skills.
Benefits
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Vacation β 120 hours per calendar year.
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Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado β 48 hours per calendar year; for employees who reside in the State of Washington β 56 hours per calendar year.
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Holiday pay, including Floating Holidays β 13 days per calendar year.
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Work, Personal and Family Time - up to 40 hours per calendar year.
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Parental Leave β 480 hours within one year of the birth/adoption/foster care of a child.
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Bereavement Leave β 240 hours for an immediate family member; 40 hours for an extended family member per calendar year.
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Caregiver Leave β 80 hours in a 52-week rolling period.
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Volunteer Leave β 32 hours per calendar year.
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Military Spouse Time-Off β 80 hours per calendar year.