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Genomic Program Manager Jobs in Michigan (NOW HIRING)

Lead lifecycle management of current and future molecular diagnostic products. * Develop ... Translate complex molecular biology, genomics, clinical validation studies, and health economic ...

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Genomic Program Manager information

What is a genomic program manager?

Genomic Program Managers are professionals who oversee and coordinate projects related to genomics, such as research studies, clinical trials, or implementation of genomic technologies. They are responsible for planning, managing resources, ensuring compliance with regulations, and facilitating communication among multidisciplinary teams. Their role bridges the gap between scientific research and operational execution, ensuring that genomic initiatives are delivered efficiently and effectively.

What are the key skills and qualifications needed to thrive as a genomic program manager?

To thrive as a Genomic Program Manager, you need expertise in genomics or genetics, program management experience, and typically an advanced degree in life sciences or a related field. Familiarity with bioinformatics tools, data analysis platforms, and regulatory compliance systems is often required. Strong leadership, communication, and stakeholder management skills help drive cross-functional collaboration and project success. These capabilities ensure effective coordination of complex genomic projects, alignment with scientific objectives, and successful delivery of program outcomes.

How does a genomic program manager typically collaborate with cross-disciplinary teams to ensure successful project outcomes?

A Genomic Program Manager routinely partners with scientists, bioinformaticians, clinicians, and data analysts to coordinate complex projects involving genomic data. They act as a bridge between different stakeholders, facilitating communication, aligning project goals, and ensuring that deliverables are met on time. Regular meetings, progress tracking, and clear documentation are essential aspects of this collaboration. By fostering a cohesive team environment and addressing any interdisciplinary challenges, the Program Manager helps ensure that projects advance efficiently and according to regulatory and scientific standards.

What job categories do people searching Genomic Program Manager jobs in Michigan look for?

The top searched job categories for Genomic Program Manager jobs in Michigan are:

What cities in Michigan are hiring for Genomic Program Manager jobs?

Cities in Michigan with the most Genomic Program Manager job openings:

Infographic showing various Genomic Program Manager job openings in Michigan as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 16% Part Time, 3% Contract, and 1% Nights. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution.

Marketing Director, Biomarkers

On-site

Full-time

This job post has expired 1 day ago. Applications are no longer accepted.


Job description

Position Summary & Accountability: 

The Marketing Director, Biomarkers, is responsible for leading the marketing strategy for Photocure's growing molecular diagnostics and biomarker portfolio (AssureMDx). This position will develop and execute integrated marketing strategies that accelerate physician adoption, support commercial growth, strengthen market access, and establish the foundation for future product expansion across the precision medicine portfolio.

This role will initially focus on commercialization of centralized laboratory-developed testing (LDT) services while supporting the long-term strategic transition toward distributed FDA-regulated in vitro diagnostic (IVD) products.


  • Photocure’s strategy is to deliver innovative diagnostic and data offerings to improve decision making in precision medicine within uro-oncology.
  • Following the acquisition of Vesica Health and AssureMDx (urine-based) biomarker, Photocure’s objective is to build a leadership position in biomarkers 
  • Need to ensure development and commercial success of AssureMDx in US market initially whilst exploring opportunities globally
  • Support commercialization of centralized laboratory-developed testing (LDT) services while supporting the long-term strategic transition toward distributed FDA-regulated in vitro diagnostic (IVD) products


Responsibilities:  


Marketing Strategy  

  • Lead commercial launch readiness planning, including launch milestones, customer targeting, message testing, field readiness, KPI development, and post-launch performance tracking. 
  • Develop and execute comprehensive commercial marketing strategies supporting the biomarker portfolio. 
  • Build annual and multi-year strategic marketing plans aligned with corporate objectives. 
  • Identify market opportunities through customer research, competitive intelligence, physician insights, reimbursement changes and market analytics. 
  • Develop product positioning, segmentation, targeting, and messaging strategies. 
  • Analyze physician utilization trends, customer segmentation, referral behavior, and commercial performance. 
  • Develop dashboards and performance metrics that guide commercial decision making. 
  • Lead annual marketing planning and budget development. 

Product Marketing  

  • Lead lifecycle management of current and future molecular diagnostic products. 
  • Develop differentiated positioning and value propositions for physicians, hospitals, laboratories, payers, and integrated delivery networks. 
  • Partner with Clinical and Medical Affairs to translate scientific evidence into clinically meaningful marketing materials. 
  • Develop launch strategies for new products, indications, and market expansions. 
  • Create promotional materials that comply with applicable regulatory and promotional requirements. 
  • Lead development of integrated digital marketing strategies across physician and healthcare professional audiences. 

 Commercial Excellence  

  • Partner closely with Commercial Sales Leadership to develop sales enablement tools, customer messaging, objection handling resources, competitive positioning, and training programs. 
  • Oversee development and implementation of physician and patient-facing digital portals that support education, engagement, ordering workflows, and adoption. 
  • Support key account strategies for integrated health systems and Large Urology Group Practice Associations (LUGPA). 
  • Collaborate with Market Access to communicate reimbursement, clinical utility, and health economic value propositions.  

 Scientific Communications  

  • Translate complex molecular biology, genomics, clinical validation studies, and health economic evidence into compelling commercial messaging. 
  • Support development of conference materials, scientific exhibits, educational programs, and commercial publications. 
  • Collaborate with Key Opinion Leaders (KOLs) and professional societies to increase awareness of the company's diagnostic portfolio. 
  • Support guideline adoption initiatives through evidence-based marketing. 

Cross Functional Cooperation  

  • Partner effectively across Global Marketing, Sales, Medical Affairs, Clinical Affairs, Regulatory Affairs, Research & Development, Market Access, Laboratory Operations, Quality, Finance, and Executive Leadership. 

Core Competencies and necessary Skills needed:

  • Strategic thinker with an innovative mindset, strong commercial insight, and sound business acumen 
  • Strong analytical capability, including data interpretation and understanding of scientific evidence 
  • Strong KOL engagement and relationship management skills  
  • Demonstrate hands-on operating style with the ability to partner and collaborate effectively with field sales and commercial operations 
  • Excellent verbal and written communication skills  
  • Strong project management, cross-functional leadership, and stakeholder management capabilities 
  • High ownership mindset, results orientation, problem-solving ability, creativity, and resilience

Education and Experience Needed:  

  • Bachelor's degree in Life Sciences, Molecular Biology, Genetics, Marketing, Business, or related discipline  
  • Minimum of 8-12 years of progressive commercial experience within molecular diagnostics, medical devices, pharmaceuticals, or precision medicine, including previous field sales experience;  
  • Experience within urology, oncology or bladder cancer mandatory 
  • Proven Marketing strategy development and execution 
  • Experience launching and commercializing molecular diagnostic products across CLIA laboratory services, FDA-regulated IVDs, or both, strongly preferred.  
  • Experience with Medicare reimbursement, Local Coverage Determinations (LCDs), and diagnostic coding. 
  • Experience working with physician specialty societies including the American Urological Association (AUA), Society of Urologic Oncology (SUO), or related organizations. 
  • Global experience, including collaboration with European teams
  • Proven ability to work effectively across cross-functional teams