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Genomic Program Manager Jobs in Kentucky (NOW HIRING)

$169K - $253K/yr

... development programs covering autoimmune and neurologic diseases. As a key member of cross ... Identify, select, and oversee biomarker assays in biological matrices, including management of ...

Expertise in emerging functional genomics technologies is highly desirable, with a demonstrated ... Strong organizational and project management skills, with the ability to prioritize, manage ...

Purification Technician

Louisville, KY · On-site

$18.25 - $24.25/hr

Eurofins Genomics is looking for a DNA Purification Technician I/II to join our oligonucleotide ... Duties and responsibilities may evolve based on business needs and manager discretion; any ...

$55K - $89K/yr

... Program, Alabama Genomic Health Initiative, Live HealthSmart Alabama, and community- and cancer ... manager) : Hybrid Eligible #J-18808-Ljbffr

$123K - $166K/yr

... excel at managing multiple priorities, succeed in communicating with all levels within the ... Pay Range $123,100--$166,500 USD About 10x Genomics At 10x Genomics, accelerating our understanding ...

Or all of humanity?## At Illumina, we are expanding access to genomic technology to realize health ... Lead Illumina's media program, including day-to-day media engagement, journalist relationship ...

Purification Technician

Louisville, KY · On-site

$18.25 - $24.25/hr

Eurofins Genomics is looking for a DNA Purification Technician I/II to join our oligonucleotide ... Duties and responsibilities may evolve based on business needs and manager discretion; any ...

$179K - $242K/yr

At 10x Genomics, our mission is to accelerate the mastery of biology to advance human health. But ... Vendor Management: Act as the primary technical point of contact for external molding partners and ...

Yu and the Yu Lab project managers and operations team. This role will provide comprehensive ... Schedule, plan, and facilitate group and program social events. * Track and maintain the Yu lab ...

We are a market leader in automated bio sample management solutions and genomic services across ... Design, implement, and administer global compensation programs that support Azenta's business ...

Our patient data platform integrates genomics with deep, longitudinal clinical and imaging data ... We are advancing two programs for Dry Age-related Macular Degeneration (AMD) into the clinic, with ...

Experience working with large public genomics resources such as GEO, ArrayExpress, UK Biobank, All ... Experience managing and analyzing large, complex datasets across multiple research programs.

$144K - $169K/yr

The company's lead clinical programs include BH-30643, a first-in-class, macrocyclic, non-covalent ... Track sample retention and future use consent (e.g., for genomic/biomarker research) in accordance ...

This emerged from a genomic discovery made at the a top accredited University, from which the ... Career development supported through mentorship, training programs, and internal advancement ...

... program integrating artificial intelligence into soil and crop sciences. Their work would use ... genomic, nutrition, pest and disease, phenotypic, physiological, management, microbiome, soil ...

This work is carried out through established research programs, including the Center for ... genetics and genomics, human behavioral pharmacology, behavioral research, and clinical ...

Showing results 41-60

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 Kentucky look for?

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

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

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

Associate Director, Translational Research and Biomarkers

On-site

Otsuka Pharmaceutical Co., Ltd
Pharmaceutical and Medicine Manufacturing • 1 - 5K employees

$169K - $253K/yr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 6 days ago


Job description

Job Summary

We are seeking an experienced and highly motivated Translational Biomarker Scientist to support biomarker-driven drug development programs covering autoimmune and neurologic diseases. As a key member of cross-functional project teams, you will partner with Research, Preclinical, Clinical, Bioanalytical, Genomics, Regulatory, and Project teams to advance translational strategies, execute biomarker plans, and generate insights that inform critical clinical development decisions. This role provides the opportunity to drive innovative biomarker approaches and contribute to the development of novel therapies from early development through clinical proof of concept.

Key Responsibilities
  • Serve as a core translational biomarker representative on cross-functional asset teams supporting clinical development programs.
  • Contribute to the development and execution of biomarker strategies, including target engagement/pharmacodynamic (TE/PD) biomarkers, patient stratification approaches, and mechanism-of-action hypotheses.
  • Support indication and patient population selection through integration of translational and clinical biomarker data.
  • Identify, select, and oversee biomarker assays in biological matrices, including management of outsourced activities and external laboratory partners.
  • Develop biomarker analysis plans and support the generation, review, and interpretation of clinical biomarker data for interim and final study analyses.
  • Collaborate with internal and external stakeholders to ensure biomarker activities are delivered on time and meet scientific, operational, and quality expectations.
  • Contribute to biomarker-related clinical study documents, regulatory submissions, and responses to health authority requests.
  • Evaluate and implement emerging technologies, digital biomarkers, and novel assay platforms that enhance biomarker measurement and clinical trial execution.
  • Present biomarker strategies, data, and recommendations to project teams and governance committees.
Qualifications
  • PhD or MS in Immunology, Neuroscience, Molecular Biology, Genomics, Pharmacology, or a related scientific discipline.
  • Minimum of 5 years of relevant experience in translational medicine, biomarker sciences, clinical research, or clinical development within immunology and/or neurology.
  • Strong knowledge of biomarker discovery, validation, and application in clinical drug development.
  • Expertise in biochemical, molecular, cellular, and genomic technologies, including RNA-Seq, exome and whole genome sequencing, proteomics, multiplex flow cytometry, and related analytical approaches.
  • Experience utilizing bioinformatics tools and interpreting complex multi-omics datasets.
  • Understanding of digital biomarker technologies and their potential application in clinical development.
  • Knowledge of global clinical research regulations, GCP principles, and biomarker-related regulatory considerations.
  • Demonstrated ability to manage multiple priorities and operate effectively in a fast-paced, matrixed environment.
  • Strong scientific problem-solving, critical thinking, and data interpretation skills.
  • Excellent verbal and written communication skills, with the ability to communicate complex scientific concepts to both technical and non-technical audiences.
Competencies
  • Accountability for Results - Stay focused on key strategic objectives, be accountable for high standards of performance, and take an active role in leading change.
  • Strategic Thinking & Problem Solving - Make decisions considering the long-term impact to customers, patients, employees, and the business.
  • Patient & Customer Centricity - Maintain an ongoing focus on the needs of our customers and/or key stakeholders.
  • Impactful Communication - Communicate with logic, clarity, and respect.
  • Influence at all levels to achieve the best results for Otsuka.
  • Respectful Collaboration - Seek and value others’ perspectives and strive for diverse partnerships to enhance work toward common goals.
  • Empowered Development - Play an active role in professional development as a business imperative.
Salary

Minimum $169,222.00 - Maximum $253,000.00, plus incentive opportunity: The range shown represents a typical pay range or starting pay for individuals who are hired in the role to perform in the United States. Other elements may be used to determine actual pay such as the candidate’s job experience, specific skills, and comparison to internal incumbents currently in role. Typically, actual pay will be positioned within the established range, rather than at its minimum or maximum. This information is provided to applicants in accordance with states and local laws.

Application Deadline

Application Deadline: This will be posted for a minimum of 5 business days.

Company Benefits
  • Comprehensive medical
  • Dental
  • Vision
  • Prescription drug coverage
  • Company provided basic life
  • Accidental death & dismemberment
  • Short-term and long-term disability insurance
  • Tuition reimbursement
  • Student loan assistance
  • A generous 401(k) match
  • Flexible time off
  • Paid holidays
  • Paid leave programs
  • Other company provided benefits
About Otsuka

Otsuka Pharmaceutical Co., Ltd. is a global healthcare company with the corporate philosophy: “Otsuka–people creating new products for better health worldwide.” In the U.S., Otsuka is comprised of two companies, Otsuka America Pharmaceutical, Inc., and Otsuka Pharmaceutical Development & Commercialization, Inc., that share a deep commitment to the development and commercialization of innovative products in the spaces of neuroscience, nephrology, and digital medicine. Driven by our purpose to defy limitation, so that others can too, we have an unwavering belief in doing more and transcending expectations. In going above and beyond—under any circumstances—for patients, families, providers, and for each other. It’s this deep-rooted dedication that drives us to uncover answers to complex, underserved medical needs, so that patients can push past the limitations of their disease and achieve more than they thought was possible each and every day. OPDC and OAPI are indirect subsidiaries of Otsuka Pharmaceutical Company, Ltd., which is a subsidiary of Otsuka Holdings Co., Ltd. headquartered in Tokyo, Japan. The Otsuka group of companies employed 34,400 people worldwide and had consolidated sales of approximately USD 14.2 billion in 2023. We invite you to explore our open positions for an opportunity to join our 2,200 colleagues in the U.S. whose passion for our mission and pride in our company have earned us certification as a Great Place to Work by the Great Place to Work Institute.

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