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Remote Director Engineering Medical Device Jobs in Kentucky

Qualus

Senior Commissioning Engineer

Louisville, KY · On-site +1

$95K - $131K/yr

Direct and approve all testing, commissioning, startup, and verification activities for relays ... Lead coordination meetings with engineering, operations, maintenance, construction, and client ...

Qualus

Senior Commissioning Engineer

Louisville, KY · On-site +1

$95K - $131K/yr

Direct and approve all testing, commissioning, startup, and verification activities for relays ... Lead coordination meetings with engineering, operations, maintenance, construction, and client ...

micro1 AI

Medical Writing Manager

Louisville, KY · Remote

$50 - $80/hr

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Direct experience independently authoring or leading the authoring of full Clinical Study Reports ...

micro1 AI

Medical Billing Specialist

Louisville, KY · Remote

$50 - $80/hr

Remote micro1 is engaging Medical Writers / Clinical Document Authors to participate in a customer ... Direct experience independently authoring or leading the authoring of full Clinical Study Reports ...

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Remote Director Engineering Medical Device information

What does a remote director engineering medical device do?

A Remote Director of Engineering in the medical device industry oversees engineering teams and projects related to the design, development, and manufacturing of medical devices, all while working remotely. They ensure that products meet regulatory standards, manage cross-functional teams, and drive innovation from concept through to production. This role requires strong leadership, technical expertise, and experience in the medical device field, as well as excellent communication skills to coordinate with remote teams and stakeholders.

What are the key skills and qualifications needed to thrive as a remote director engineering medical device?

To thrive as a Remote Director of Engineering in Medical Devices, you need deep expertise in engineering principles, regulatory compliance (such as FDA and ISO 13485), and a relevant degree in engineering or a related field. Familiarity with product lifecycle management (PLM) systems, quality management software, and certifications like PMP or Six Sigma are highly valuable. Exceptional leadership, cross-functional communication, and strategic problem-solving skills help you effectively manage remote teams and complex projects. These capabilities ensure safe, innovative product development that complies with industry standards and drives organizational success.

What are some unique challenges faced by a remote director engineering medical device, and how can they be addressed?

A Remote Director of Engineering in the medical device field often navigates challenges such as ensuring effective collaboration across distributed teams, maintaining regulatory compliance, and overseeing complex product development cycles without onsite presence. To address these, it's important to implement robust project management tools, establish regular virtual check-ins, and foster a culture of clear documentation and accountability. Staying current with regulatory changes and leveraging digital quality management systems also help ensure that remote teams remain aligned with industry standards and deadlines.

What are popular job titles related to Remote Director Engineering Medical Device jobs in Kentucky?

For Remote Director Engineering Medical Device jobs in Kentucky, the most frequently searched job titles are:

What job categories do people searching Remote Director Engineering Medical Device jobs in Kentucky look for?

The top searched job categories for Remote Director Engineering Medical Device jobs in Kentucky are:

What cities in Kentucky are hiring for Remote Director Engineering Medical Device jobs?

Cities in Kentucky with the most Remote Director Engineering Medical Device job openings:

Remote Director Engineering Medical Device jobs near you

Senior Biostatistician (Clinical Trial Experience Required)

CTI

Covington, KY • On-site, Remote

Full-time

Medical, PTO

Posted 19 days ago

Job description

What You'll Do:
  • Assist with the development and modification of department SOPs and work instructions
  • Assist with training new Biostatistics employees; mentor and assist junior level Biostatisticians
  • Develop study bids and changes in scope for Biostatistics tasks in response to prospective client's request for proposals (RFPs)
  • Attend and present the Biostatistics study execution tasks at capabilities presentations.
  • As the lead Biostatistician on the studies to which you are assigned, perform, or oversee the following tasks:
    • Act as primary statistical contact for internal and external project team members
    • Manage projects to ensure statistics tasks are performed within the entire project timeline. Keep Biostatistics management aware of changes to project timelines
    • Proactively identify and communicate changes in scope to the clinical project manager and Biostatistics management
    • Review case report forms (CRFs) and completion instructions
    • Give input to database design and data edit considerations necessary to collect and clean data
    • Develop or review Interim Analysis Plans (IAPs) and Statistical Analysis Plans (SAPs) as needed per the protocol
    • Develop or review program specifications - SDTM and ADaM dataset specifications and mock tables, listings, and figures (TLFs) - needed to perform the analysis defined in the IAP/SAP
    • Perform the statistical analysis by independently programming derived datasets and TLFs and validate the developer's corresponding programs per department SOPs
    • Review programming of other team members
    • Develop or review statistical methods and results sections of statistical reports, clinical study reports (CSRs), or publications
    • Plan and design clinical studies, including:
      • overall study design development
      • outcome / endpoint determination
      • power analysis / sample size estimation reports
      • randomization and blinding procedures development
      • statistical methods section development in the protocol
    • Develop or review Randomization Plans, and randomization programs or lists
  • Carry out all activities according to CTI SOPs and project-specific conventions within the framework of Good Clinical Practice (GCP) / International Conference on Harmonization (ICH) guidelines
  • Rely on instructions and Biostatistics SOPs to ensure timely, standard, quality deliverables to customers
  • Maintain accurate records of all work performed and ensure all relevant statistics documents are filed in the eTMF per the project-specific eTMF Plan
  • Provide input to and participate in departmental meetings

What You'll Bring:
  • At least 4 years of related biostatistics experience in either a pharmaceutical or CRO environment or other relatable statistical experience
  • Master's degree in Biostatistics, Statistics, or related field
  • CDISC, SDTM, and ADaM dataset mapping experience
  • BLA/NDA Submission experience; regulatory representation (i.e., meeting preparation/attendance, follow-up with regulatory communication) preferred
  • Therapeutic experience in transplantation, autoimmune diseases, kidney and liver disease, oncology and rare disease preferred
  • Experience providing statistical consulting to internal/external clients preferred

About CTI
CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development, from drug concept to commercialization. CTI is headquartered in the Greater Cincinnati, OH region with global operations in collaboration with pharmaceutical, biotechnology, and medical device firms. For more information, visit www.ctifacts.com
Why CTI?
  • Advance Your Career - We support career progression through a structured mentoring program and leadership courses that provide the support needed to grow. We also value ongoing education and training through tuition reimbursement and a dedicated training department.
  • Join an Award-Winning and Valued Team - We have an award-winning unparalleled culture that can be felt by our employees across 60 countries. We support a work-life balance and the importance of time with family by offering generous health benefits and vacation packages, hybrid work from home opportunities, and paid parental leave. We also encourage care for the world around us through our unique CTI Cares program.
  • Make a Lasting Impact - We focus on moving medicine forward by working on treatments for chronically and critically-ill patients, who depend on us to bring life-changing therapies to market.

Important NoteIn light of recent increase in hiring scams, if you're selected to move onto the next phase of our hiring process, a member of our team will reach out to you directly from an @ctifacts.com email address to guide you through our interview process. Please ensure you are applying for jobs directly on our website (www.ctifacts.com) or from our verified LinkedIn page.
Please Note
  • We will never communicate with you via Microsoft Teams or text message
  • We will never ask for your bank account information at any point during the recruitment process

Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.

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