Senior Study Director, Rare Disease Translational Center

JAX; Bar Harbor (ME); On-site; USD 99,000 - 166,000; Full time

Job summary

The Jackson Laboratory in Bar Harbor, Maine is seeking a Senior Study Director for the Rare Disease Translational Center. You will lead multidisciplinary teams to drive complex preclinical studies, ensuring GLP/ICH compliance and high-quality data delivery for rare disease models and therapies.

You will provide strategic direction, oversee study design and execution, mentor staff, and liaise with clients to meet project objectives and regulatory expectations.

Qualifications

• Extensive experience in scientific research and leadership roles within pharma/biotech/CRO.
• Proven track record in managing complex research projects and teams.
• Strong understanding of GLP, ICH, and regulatory interactions.

Responsibilities

• Develop strategic plans for execution of scientific studies, including design and resource allocation.
• Lead and oversee all aspects of studies, ensuring timelines, budgets, and regulatory compliance.
• Provide guidance across study lifecycles: protocols, data analysis, and result interpretation.

Skills

Scientific leadership

Project management

Regulatory knowledge

Data analysis

Communication

Education

Doctorate (PhD) in a relevant field

Tools

SAS

R

SPSS

Job description

Senior Study Director, Rare Disease Translational Center# Review our Cookie Policy HERE### Senior Study Director, Rare Disease Translational CenterApply: Bar Harbor, Maine: Posted 3 Days Ago: JR006347**Job Summary** Rare diseases affect millions of people, yet most have no approved treatments. The Rare Disease Translational Center (RDTC) at The Jackson Laboratory is working to change that by building clinically relevant mouse models and using them to test the therapies that could reach patients next, including emerging approaches such as gene therapy and RNA-based treatments. We’re looking for a motivated, detail-oriented full-time Senior Study Director to join our team in Bar Harbor, Maine. The Rare Disease Translational Center supports the overall mission of The Jackson Laboratory: To discover precise genomic solution for disease and empower the global biomedical community in the shared quest to improve human health. The RDTC works directly with foundations and their associated teams of basic and clinical researchers to generate custom mouse and cell based/in vitro models with clinical mutations to treat and cure rare diseases. This position is an exciting opportunity to work directly with the Center in supporting this mission. As a Senior Study Director, you will play a critical role in leading and overseeing scientific studies within a research or laboratory environment. Building upon your extensive experience and expertise, you will be responsible for providing strategic direction, scientific guidance, and leadership to multidisciplinary project teams. Your primary objective will be to ensure the successful execution of complex research projects, driving the delivery of high-quality data and achieving project objectives in compliance with regulatory standards and client expectations. **Key Responsibilities & Essential Functions** • Develop strategic plans for the execution of scientific studies, including study design, methodology, and resource allocation, in alignment with organizational goals and objectives. • Lead and oversee all aspects of assigned studies, including study planning, execution, and reporting, ensuring adherence to timelines, budgets, and regulatory requirements. • Provide scientific guidance and expertise throughout the study lifecycle, including protocol development, data analysis, and interpretation of results, to drive decision-making and project success. • Ensure studies are conducted in accordance with relevant regulatory requirements, such as Good Laboratory Practice (GLP), International Conference on Harmonisation (ICH) guidelines, and other applicable standards. • Implement robust quality control measures to maintain the integrity, accuracy, and reliability of study data, overseeing documentation and record-keeping practices to ensure compliance with regulatory standards. • Lead and mentor multidisciplinary project teams, including scientists, technicians, and support staff, to foster a collaborative and high-performing work environment, promoting professional growth and development. • Oversee data analysis activities, ensuring robust statistical analysis methodologies are applied, and prepare comprehensive study reports for internal review and client submission, with a focus on accuracy, clarity, and scientific rigor. • Identify and mitigate potential risks and challenges that may impact study timelines, data quality, or regulatory compliance, implementing proactive measures to address issues and drive project success. • Other duties as assigned. **Knowledge, Skills, and Abilities** • Extensive experience in scientific research, project management, and leadership roles within a pharmaceutical, biotechnology, or contract research organization (CRO) environment, with a demonstrated track record of success in leading complex research projects. • Exceptional leadership and team-building skills, with the ability to inspire and motivate multidisciplinary teams to achieve project objectives and deliver high-quality results. • Strategic mindset with the ability to develop and execute strategic plans, prioritize tasks, and allocate resources effectively to achieve organizational goals and objectives. • Thorough understanding of regulatory requirements governing preclinical and clinical research studies, including GLP, ICH guidelines, and other relevant regulations, with experience in regulatory interactions and submissions. • Strong analytical skills with proficiency in data analysis and interpretation, including advanced statistical analysis methodologies and software tools (e.g., SAS, R, SPSS). • Excellent verbal and written communication skills, with the ability to convey complex scientific concepts clearly and effectively to diverse audiences, including clients, internal stakeholders, and regulatory agencies. • Strategic problem-solving abilities, with a proactive approach to identifying and addressing challenges, implementing effective solutions, and driving continuous improvement initiatives. • Meticulous attention to detail and a commitment to maintaining the highest standards of data integrity, accuracy, and compliance in all aspects of study conduct and reporting. • Flexibility and adaptability to changing priorities, deadlines, and client requirements in a dynamic and fast-paced work environment, with the ability to thrive under pressure and deliver results\\*Advanced knowledge of genetic and molecular techniques relevant to rare disease research **Minimum Requirements** Experience Required/Preferred: 9 years/ 12 yearsEducation Required/Preferred: Doctorate/Doctorate Pay Range: $98,885 - $165,554, pay is determined by years of experience **About JAX:**The Jackson Laboratory is an independent, nonprofit biomedical research institution with a National Cancer Institute-designated Cancer Center and nearly 3,000 employees in locations across the United States (Maine, Connecticut, California, New York, Florida), Japan and China. Its mission is to discover precise genomic solutions for disease and empower the global biomedical community in the shared quest to improve human health. Founded in 1929, JAX applies over nine decades of expertise in genetics to increase understanding of human disease, advancing treatments and cures for cancer, neurological and immune disorders, diabetes, aging and heart disease. It models and interprets genomic complexity, integrates basic research with clinical application, educates current and future scientists, and provides critical data, tools and services to the global biomedical community. For more information, please visit www.jax.org. **EEO Statement:***The Jackson Laboratory provides equal employment opportunities to all employees and applicants for employment in all job classifications without regard to race, color, religion, age, mental disability, physical disability, medical condition, gender, sexual orientation, genetic information, ancestry, marital status, national origin, veteran status, and other classifications protected by applicable state and local non-discrimination laws.*