Director, Scientific Statistical and Data Coordinating Center

Emmes; Rockville (MD); Remote; USD 180,000 - 250,000; Full time

Benefits offered by this job

Work From Home Anywhere in the US

Flexible Approved Time Off

Tuition Reimbursement

401k Retirement Plan

Maternal/Paternal Leave

Job summary

Emmes is seeking a Scientific Director for the Statistical and Data Coordinating Center (SDCC). The role is US-Remote and focuses on leading large, complex government-sponsored clinical trials with expertise in biostatistics, vaccine and infectious disease programs, and line management at senior levels.

You will build external and internal relationships, contribute to business development, and guide study design, analysis, and manuscript development while ensuring data quality, dissemination,

Qualifications

• Master's degree in biostatistics or related field with clinical research focus.
• PhD preferred for leadership in government-sponsored trials.
• Strong analytical, writing and presentation capabilities.
• Excellent stakeholder management and communication skills.
• Experience leading multi-center clinical research programs.

Responsibilities

• Lead large multi-center, multi-protocol clinical trial programs supported by US Government.
• Provide statistical input, oversight, and guidance for study design and analysis.
• Develop study protocols and manuscripts for peer-reviewed journals.
• Build relationships with government sponsor representatives and internal executives.

Skills

Problem solving

Business judgment

Communication skills

Facilitation

Leadership

Writing skills

Presentation skills

Listening skills

Relationship management

Education

Master's degree in biostatistics, epidemiology, public health or related field

PhD preferred

Job description

Scientific Director, Statistical and Data Coordinating Center

US Remote

Emmes Group: Building a better future for us all.

Emmes Group is transforming the future of clinical research, bringing the promise of new medical discovery closer within reach for patients. Emmes Group was founded as Emmes more than 47 years ago, becoming one of the primary clinical research providers to the US government before expanding into public-private partnerships and commercial biopharma. Emmes has built industry leading capabilities in cell and gene therapy, vaccines and infectious diseases, ophthalmology, rare diseases, and neuroscience.

We believe the work we do will have a direct impact on patients’ lives and act accordingly. We strive to build a collaborative culture at the intersection of being a performance and people driven company. We're looking for talented professionals eager to help advance clinical research as we work to embed innovation into the fabric of our company. If you share our motivations and passion in research, come join us!

Primary Purpose

The Scientific Director, Statistical and Data Coordinating Center (SDCC), will lead large complex multi-center and multi-protocol clinical trial programs that are sponsored by the US Government, including the National Institutes of Health. The scientific director will build and maintain relationships with external government sponsor representatives and internal executives to ensure long-term program success. This role will also support business development activities to help expand Emmes’ government business and additional corporate initiatives. This role also requires therapeutic expertise in one or more areas that align with Emmes research focus, including vaccine and infectious disease, ophthalmology, cell and gene therapy, organ transplantation, neuroscience, substance use, and maternal and child health. Expertise in biostatistics to provide statistical input, oversight, senior review, and guidance is a key aspect of the role.

Responsibilities

• Oversight and innovation for all aspects of the SDCC research program to ensure successful project implementation, data management, analysis, and dissemination of results.
• Key responsibilities of the Scientific Director on the research program includes development of study protocols, statistical expertise in the areas of design and analysis, and lead the development of manuscripts for peer-reviewed journals.
• Establishes and maintain relationships with external government sponsor representatives and internal executives.
• Supports corporate initiatives including business development activities to expand government business.

Qualifications

• Minimum of a Master's degree in biostatistics, epidemiology, public health or another field relevant to clinical research and at least 8 years of clinical research experience. PhD Preferred.
• Demonstrated success overseeing a portfolio of clinical research in the specific therapeutic area with a typical tenure of at least 5 years research portfolio management experience.
• Deep experience leading clinical research projects with experience in or working knowledge of unique challenges and considerations of disease research.
• Working knowledge of the principles of clinical research management.
• Demonstrated strong problem solving and analytical skills, combined with business judgment.
• Effective communication skills, including strong presentation, writing, and listening skills.
• Ability to facilitate discussion with leadership and stakeholders.
• Excellent customer service and relationship management skills.
• Strong analytical skills.
• Therapeutic experience in vaccine and infectious disease required

Why work at Emmes?

At Emmes, your actions and hard work will have a direct impact on public health initiatives, both globally and in our local communities with opportunities for volunteerism through our Emmes Cares community engagement program. We offer a competitive benefits package focused on the health and needs of our growing workforce, including:

• Flexible Approved Time Off
• Tuition Reimbursement
• 401k Retirement Plan
• Work From Home Anywhere in the US
• Maternal/Paternal Leave
• Casual Dress Code & Work Environment

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The Emmes Company, LLC is an equal opportunity employer and does not discriminate in its selection and employment practices. All qualified applicants will receive consideration for employment without regard to disability or protected veteran status.

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