Current jobs related to Sr. Manager, Clinical Affairs - Carlsbad - Carlsmed


  • Carlsbad, United States Meet Full time

    A growing medical device company based in North San Diego county is hiring a Regulatory Affairs Manager for their QA/RA department. The company is developing breakthrough products for the treatment of cardiac arrhythmias and will be commercializing several new products by the end of this year and early next.The RA Manager will be responsible for leading the...


  • Carlsbad, United States Meet Full time

    A growing medical device company based in North San Diego county is hiring a Regulatory Affairs Manager for their QA/RA department. The company is developing breakthrough products for the treatment of cardiac arrhythmias and will be commercializing several new products by the end of this year and early next.The RA Manager will be responsible for leading the...


  • Carlsbad, United States Meet Full time

    Regulatory Affairs ManagerMeet is seeking a highly skilled Regulatory Affairs Manager to lead the regulatory strategy and manage submissions for new product launches. This is a hands-on role that requires a deep understanding of regulatory requirements and processes, particularly in premarket submissions.Key Responsibilities:Develop and implement regulatory...


  • Carlsbad, United States Alphatec Spine Full time

    Job DescriptionJob DescriptionThe Senior Regulatory Affairs Specialist will be responsible for the development of submissions for domestic and international clearances; as well as the support of daily activities related to new product development, change control, and regulatory product submissions.Essential Duties and Responsibilities Collaborates as a core...


  • Carlsbad, United States Internetwork Expert Inc Full time

    Position Overview:The role involves the formulation of regulatory submissions for both domestic and international spinal product approvals. Collaborate with spinal product design teams on change management and regulatory documentation.Key Responsibilities:Provide guidance on domestic and international regulatory strategies for products, including spinal...


  • Carlsbad, United States Danaher Corporation Full time

    Position Overview:The Regulatory Affairs Associate plays a crucial role in ensuring compliance with regulatory standards and facilitating the approval process for design documentation.Key Responsibilities:- Conduct regulatory assessments and develop plans for design control activities.- Ensure adherence to regulatory compliance requirements across US, EU,...


  • Carlsbad, New Mexico, United States Clinical Management Consultants Full time

    Job Summary: We are seeking a highly skilled Inpatient Clinical Pharmacist to join our team at Clinical Management Consultants. As a Clinical Pharmacist, you will play a critical role in supporting our hospital's pharmaceutical efforts and providing high-quality patient care.Key Responsibilities:Monitor patient progress and evaluate the appropriateness and...


  • Carlsbad, New Mexico, United States Clinical Management Consultants Full time

    Job Summary: We are seeking a highly skilled Inpatient Clinical Pharmacist to join our team at Clinical Management Consultants. As a key member of our healthcare team, you will play a critical role in providing exceptional patient care and supporting our hospital's pharmaceutical efforts.Key Responsibilities:Monitor patient progress and evaluate the...


  • Carlsbad, United States Thermo Fisher Scientific Full time

    Thermo Fisher Scientific is seeking a seasoned professional in Regulatory Affairs to become a vital member of the Bio-Sciences Division team. This role offers the flexibility of remote work. Key Responsibilities:Formulate and execute comprehensive global regulatory strategies.Oversee the preparation of FDA pre-submission documentation and coordinate...


  • Carlsbad, United States Meet Full time

    Job SummaryWe are seeking a highly skilled Regulatory Affairs Manager to join our QA/RA department. As a key member of our team, you will be responsible for leading the regulatory strategy and managing submissions for new product launches.Key ResponsibilitiesDevelop and implement regulatory strategies for new product development and...


  • Carlsbad, United States Internetwork Expert Inc Full time

    Position Overview:The Senior Regulatory Affairs Specialist will be responsible for crafting regulatory submissions for both domestic and international spinal product approvals. This role will also involve collaborating with spinal product design teams on change control processes and regulatory submissions.Key Responsibilities:1. Provide regulatory expertise...


  • Carlsbad, United States LHH Recruitment Solutions Full time

    Job DescriptionJob DescriptionLHH Recruitment Solutions is seeking a highly skilled Regulatory Affairs Specialist with expertise in the medical device industry for a minimum 6-month contract role. As part of a Fortune 500 company, you will play a crucial role in ensuring regulatory compliance and supporting product development within the medical equipment...


  • Carlsbad, United States Alphatec Spine Full time

    Job DescriptionJob DescriptionPrimary responsibilities include the development of submissions for domestic and international clearances. Additionally, will assist to support daily activities such as new product development, change control, and post market surveillance.Essential Duties and Responsibilities Collaborates as a core team member on new product...


  • Carlsbad, United States Spinal Elements Full time

    About Spinal ElementsSpinal Elements is a Carlsbad, California-based medical device company focused on the design, development, and commercialization of a comprehensive portfolio of systems, products, and technologies for spine surgery procedures. A leading designer, developer, manufacturer, and marketer of innovative medical devices used in spinal surgical...


  • Carlsbad, United States Spinal Elements Full time

    About Spinal ElementsSpinal Elements is a leading medical device company based in Carlsbad, California, specializing in the design, development, and commercialization of innovative systems, products, and technologies for spine surgery procedures.The company combines cutting-edge medical device technologies, biologics, and instrumentation to create positive...


  • Carlsbad, United States Spinal Elements Full time

    About Spinal ElementsSpinal Elements is a leading medical device company based in Carlsbad, California, dedicated to designing, developing, and commercializing innovative systems, products, and technologies for spine surgery procedures. With a comprehensive portfolio of advanced spinal implant technologies, the company has established a reputation for...


  • Carlsbad, New Mexico, United States Clinical Management Consultants Full time

    Acute Care Pharmacist OpportunityWe are seeking a highly skilled Inpatient Clinical Pharmacist to join our team at a state-of-the-art hospital in Southern New Mexico.This 180+ bed Level IV Trauma Acute Care Hospital is committed to providing exceptional patient care and is looking for a Clinical Pharmacist to support their pharmaceutical efforts.The...

  • Clinical Pharmacist

    3 weeks ago


    Carlsbad, New Mexico, United States Clinical Management Consultants Full time

    Job Summary: We are seeking a highly skilled Inpatient Clinical Pharmacist to join our team at Clinical Management Consultants. As a key member of our healthcare team, you will play a critical role in providing exceptional patient care and supporting our hospital's pharmaceutical efforts.Key Responsibilities:Monitor patient progress and evaluate the...


  • Carlsbad, United States Spinal Elements Full time

    About Spinal ElementsSpinal Elements is a leading medical device company focused on the design, development, and commercialization of innovative systems, products, and technologies for spine surgery procedures.The company combines cutting-edge medical device technologies, biologics, and instrumentation to create positive surgical outcomes that exceed surgeon...


  • Carlsbad, United States Vaco Full time

    Summary We are seeking an experienced Sr Manager to lead our client's Enterprise Solutions Engineering team, with a focus on technical design, development, and support of our ERP system and business applications. The ideal candidate will have a strong background in Dynamics 365 Finance and Operations (F&O), expertise in X++, and a proven track record of...

Sr. Manager, Clinical Affairs

4 months ago


Carlsbad, United States Carlsmed Full time
Job DescriptionJob DescriptionSalary:

About Carlsmed                                                                                                                            

Our mission is to improve outcomes and decrease the cost of healthcare for spine surgery and beyond. The Carlsmed aprevo® personalized surgery platform is designed to improve the standard of care for spine surgery one patient at a time.

 

Position Description

Carlsmed seeks an experienced clinical affairs manager to oversee post market studies of surgical implants for adult spinal disorders.  The current primary project is the ongoing COMPASS™ multi-center post market observational registry.   COMPASS (Clinical Outcome Measures in Personalized aprevo® Spine Surgery) will follow up to 300 subjects for 2 years post-surgery.

 

Responsibilities

  • Manage clinical study operations at 15+ study sites in the US.
  • Daily field activities and communications with study sites (Principal Investigators, study coordinators), Institutional Review Boards (local and central IRBs), and in-house partners (Data Management, Medical Affairs, Accounting).
  • Supervise clinical research associates to achieve project milestones.
  • Oversee site onboarding, initiation/training, interim monitoring, and closeout.
  • Support IRB submissions, patient enrollment, case report form completion and data queries.
  • Create or update protocols and related documents (Case Report Forms, site and sponsor guidelines, site regulatory and subject binders, work instructions, monitoring reports, study agreements/budgets.
  • Maintain electronic records including study-wide and site-specific documents.
  • Administer electronic data capture (EDC) system for data entry by study site staff.
  • Author study progress reports and monthly newsletters to study site staff.
  • Review invoices from study sites and vendors.
  • Support regulatory authority audits of study sites and/or sponsor as necessary.

 

Qualifications

  • Minimum: Bachelor’s degree in life science
  • Minimum 10 years clinical study experience
  • Knowledge of spine surgery and/or orthopedics
  • GCP trained and knowledge of FDA and ICH requirements
  • Institutional Review Board submissions and related materials (protocol, ICF, CRFs)
  • User/administrator of clinical Electronic Data Capture systems
  • Available for domestic travel 5-10 days per month


Skills

  • Excellent written communication skills, including reviewing and editing others’ work
  • Strong computer software skills (MS Word, Excel, Outlook, PowerPoint, and Access experience)
  • Strong communication and presentation skills
  • Ability to manage subordinates while independently performing high quality work
  • Continuous issue detection and resolution

 

Equal Opportunity Employer

Carlsmed is an equal opportunity employer.  All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.  Carlsmed is committed to providing reasonable accommodations for candidates with disabilities in our recruiting process. If you need any assistance or accommodations due to a disability, please let us know.

 

Compensation

We are pleased to provide a competitive salary and benefits. Our benefits reflect our investment in the overall health and well-being of our employees and their families. including paying 100% of monthly healthcare, dental & vision insurance premiums, a 401(k) plan with employer matching and unlimited PTO. The expected annual pay range is $130k to $165k. Compensation may vary based on related skills, experience, and relevant key attributes.