Senior Clinical Affairs PM - Medical Devices
Intuitive
Intuitive is looking for a Senior Project Manager for Clinical Affairs to oversee clinical studies and regulatory submissions. This role demands leadership in project management, collaboration with cross-functional teams in a fast-paced environment, and adherence to regulatory standards. The ideal candidate will have a Bachelor’s degree in Life Sciences or Engineering, with extensive experience in clinical project management. Join us as we innovate healthcare technologies and improve patient outcomes. #J-18808-Ljbffr Intuitive
- ...Primary Function of Position The Senior Project Manager, Clinical Affairs, plays a pivotal role in supporting... ...Data Management, Biostatistics, and Medical Sciences to ensure timely, consistent... ...least 3 years focused on medical device development. Experience acting as...SeniorMedical deviceLocal areaWorldwideFlexible hours
- Intuitive is seeking a Senior Project Manager for Clinical Affairs to oversee and coordinate clinical studies, ensuring timely deliverables aligned... ...clinical project management, particularly within the medical device field. Remote work options are available as part of...SeniorMedical deviceRemote work
- ...reports to Manger/Sr. Manager, Medical Sciences and requires a... ...medical literature, data from clinical trials and pre-clinical studies... ...therapeutic areas, competitor devices, current clinical/market developments... ...broader Clinical/Medical Affairs activities such as Regulatory...SeniorMedical deviceLocal areaWorldwide
$105k - $120k
...strengths of Quidel Corporation and Ortho Clinical Diagnostics, creating a world‑... ...healthier future for all. The Role Senior Regulatory Affairs Specialist. This role manages regulatory... ...of new in vitro diagnostics and medical devices worldwide. Responsibilities include...SeniorMedical deviceWork experience placementWork at officeRemote workWorldwideHome officeNight shift$131.56k - $164.45k
Sonova Group is seeking a Senior Manager, Clinical Trials, responsible for overseeing complex, multi-country clinical trials for medical devices. This role demands expertise in regulatory compliance and project management to drive strategic directions aligned with business...SeniorMedical device- Sonova USA Inc. is seeking a Senior Manager, Clinical Trials to own the strategy for late-phase studies while ensuring cross-functional alignment. You will oversee complex clinical trials for medical devices globally. The ideal candidate has 8+ years of experience leading...SeniorMedical deviceRemote work
- BioRobotics is seeking a Senior Regulatory Affairs Specialist at their California headquarters to oversee regulatory affairs in urological surgery... ...will be essential in driving continuous improvement for medical devices. Join us to make a meaningful difference in the treatment...SeniorMedical device
$148.55k - $174.77k
...suffering from BPH are treated? Join us as a Senior Regulatory Affairs Specialist and be at the forefront of regulatory science for medical robotics. Your mission? To support a deep... ...for new and modified Class II and III devices and preparing and submitting regulatory...SeniorMedical device$131.56k - $164.45k
...connection - from personal audio devices and wireless communication... ...span both consumer and medical solutions and the freedom... ...and every story matters. Senior Manager, Clinical Trials 163618 The Senior Manager... ...Evaluation, Medical Affairs, and the Clinical Development...SeniorMedical deviceTemporary workLocal areaRemote workFlexible hours- Intuitive is seeking a Senior Manager of Clinical Affairs to oversee clinical strategies for innovative technologies. The successful candidate will manage clinical trials, publications, and team development while collaborating across functions to optimize study strategies...Senior
$80 - $100 per hour
...partnering with a scaling Class III MedTech business to hire a Senior Regulatory Affairs Specialist (Contractor). This is a fantastic opportunity... ...partners Managing a wide variety of RA tasks across Medical Devices Ensuring compliance with Class III device regulatory...SeniorMedical deviceHourly payPermanent employmentFull timeContract workFor contractorsRemote work$100.32k - $125.4k
Senior Specialist, International Regulatory Affairs Job ID: 164201 Advanced Bionics is seeking a Senior Specialist, International Regulatory Affairs to... ...support global regulatory activities for Class III medical devices. This role is responsible for helping obtain and...SeniorMedical deviceTemporary workWork experience placementWork at officeLocal areaFlexible hours- LivaNova is seeking a Medical Science Liaison based in California to develop collaborations... ...stakeholders and support ongoing clinical development. The ideal candidate will... ...three years of experience in medical affairs in the medical device industry. This role emphasizes...SeniorMedical deviceRemote jobFlexible hours
- ZEISS Meditec Inc. in the United States seeks a Senior Advisor of Regulatory and Clinical Affairs to guide regulatory and clinical strategies for CZM's... ...timely, compliant commercialization of ophthalmic medical devices. You will lead FDA submissions (510(k), PMA, IDE),...Medical device
- Regulatory Affairs Specialist - Medical Devices Position: Regulatory Affairs Specialist - Medical Devices Location... ...with R&D, Quality, and Clinical teams to support product development... ...Cross-Functional Collaboration Skills Seniority level: Associate Job function: Manufacturing...Medical deviceContract work
- BioRobotics is looking for a Senior Product Manager to lead the software product strategy... ...while working closely with clinical and engineering teams. The successful candidate... ...software product management within the medical device field, and possess a Bachelor's degree...SeniorMedical device
- ...Location/Site: Irvine, CA Role Overvie wThe Senior Biomedical Engineer is a subject matter... ...for biocompatibility of ophthalmic medical devices, with a primary focus on intraocular... ...cross-functionally with R&D, Regulatory Affairs, Quality, Manufacturing, and Supplier Quality...SeniorMedical device
- ...Role Senior Manager/ AD, Regulatory Strategy Location Bay Area (Hybrid) About the Organization... ...Our client is a well‑funded, pre‑IPO clinical‑stage biotechnology company focused on... ...degree preferred. 10+ years of Regulatory Affairs experience within the biotechnology or pharmaceutical...SeniorRemote work
$89.2k
...About the role This role is for a Senior Quality Engineer supporting Boston Scientific... ...Manufacturing, Supply Chain, Regulatory Affairs, Research and Development (R&D), and other... .... Minimum of 5 years’ experience in the medical device or pharmaceutical industry. Strong...SeniorMedical device$114k - $228k
...Abbott Vascular is seeking a Regulatory Affairs Manager to join the Santa Clara, CA team. You will combine scientific, regulatory, and business insights to enable products that meet global requirements, mentoring colleagues and guiding cross-functional projects. Base pay...Medical device- OLSA Resources, Inc. is seeking a Regulatory Affairs Specialist based in California, Missouri, responsible for managing government interactions concerning approval processes for medical devices. Candidates should possess extensive experience in authoring PMA supplements...Medical device
- AbbVie is seeking a Senior Quality Engineer to oversee external product quality assurance for medical devices manufactured by third parties. This role involves managing CMOs and suppliers, ensuring product compliance, and supporting new product introductions. The ideal...SeniorMedical device
$91k - $125k
...Senior Business Development Specialist Field Role - Los Angeles Area Are you passionate... ...programs and value‑added services to HCP clinics to support adoption and engagement.... ...in business development, sales, or the medical device industry OR 3+ years of clinical audiology...SeniorMedical deviceTemporary workRemote workFlexible hours$92k - $130k
...to partner with cardiologists and clinical teams to transform patient care with devices supported by clinical evidence.... ...part of our inspiring journey. The Senior Microbiologist provides technical... ...monitoring programs supporting medical device manufacturing. This role leads...SeniorMedical device- Abbott Laboratories is searching for a Senior Systems Engineer in California to focus on system requirements and oversee interdisciplinary collaboration to enhance system designs. The role involves substantial system engineering practices and technical support to ensure...SeniorMedical device
$75.1k
About the Role Senior Product Analyst - 12 Month Defined Term Position The role is based... ...regulatory requirements for medical device complaint handling and regulatory reporting... ...safety and business operations. Apply clinical knowledge related to product applications...SeniorMedical deviceWork at officeRelocation package3 days per week- PROCEPT BioRobotics is seeking a Clinical Specialist to deliver product training and in-procedure support. The role involves ensuring... ..., strong communication skills, and a solid understanding of medical devices and robotics. Frequent travel is required as part of the job...Medical device
- ...Client: Leader in the medical device manufacturing industry Location: Brea, CA 92821 Position Overview: The Sr. Payroll Analyst is responsible for overseeing and executing payroll functions to ensure timely and accurate payment to associates. This role includes leading...SeniorMedical deviceWork at officeLocal area
$135.1k - $225.1k
...partner cross‑functionally with commercial, medical/clinical, regulatory, legal, and HR teams to... ...or related function within the medical device or pharmaceutical industries;... ...marketing, commercial operations, medical affairs, and other cross‑functional leaders. You...SeniorMedical deviceHome officeFlexible hours- ...across hospitals, nursing units, and physician teams, focusing on medical device implementations. The ideal candidate brings oncology and... ...to assess education needs, deliver clear instruction, answer clinical questions, and provide updates and feedback to clients during...Medical device
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