Overview
Join to apply for the Associate Director Clinical - Science & Medicine role at Signant Health .
Signant Health is a global evidence generation company helping customers digitally enable their clinical trial programs, meeting patients where they are, and driving change through technology and innovations. Working at Signant Health places you at the heart of a high-growth, dynamic industry.
About the Role
The Associate Director, Clinical supports strategic initiatives within the Science and Medicine department and the DHS group, aligning scientific activities with business objectives and corporate growth strategies. The Associate Director helps implement scientific initiatives and key departmental projects, contributes to thought leadership, ensures scientific quality, and represents the company as a scientific expert in selected forums.
What You’ll Do
- Support strategic initiatives for the Science and Medicine department and DHS group, aligning scientific activities with business objectives and corporate goals. Collaborate with the Sales team to define and execute high-impact strategies that increase win rates and secure new opportunities.
- Manage and develop junior clinical scientists, fostering scientific excellence, innovation, and professional growth.
- Support the Director and leadership team by contributing to departmental planning, cross-functional initiatives, and key projects.
- Contribute to thought leadership initiatives, including scientific publications, presentations, and external collaborations to enhance the company\'s scientific reputation.
- Work with business development, marketing, and commercial teams to support partnerships, client engagements, and scientific communications.
- Ensure scientific and clinical quality in project execution and interpretation, providing guidance on clinical and scientific issues and reviewing methodologies and deliverables.
- Represent the company at Investigator meetings, scientific conferences, industry meetings, and with stakeholders as a scientific expert.
- Collaborate with cross-functional teams, including Operations, Product Development, and Regulatory Affairs, to implement clinical and scientific activities aligned with business goals.
- Monitor scientific trends, industry developments, and competitive activities to inform departmental priorities and support the company\'s scientific position.
- Support strategies to ensure regulatory compliance and industry standards while maintaining scientific integrity across projects.
Decision Making and Influence
Exercise sound decision-making on scientific implementation and prioritization to balance scientific quality with business objectives.Influence project teams by effectively communicating scientific concepts and their business implications.Provide reliable scientific guidance that informs departmental initiatives and project direction.Contribute to innovation through evaluation of relevant technologies, methodologies, and therapeutic approaches.Develop relationships with scientific peers, academic institutions, and industry partners to support the company\'s scientific initiatives.What You Bring
MD, PhD, PharmD, or equivalent advanced degree in a relevant scientific or medical field.Minimum of 7+ years of experience in clinical research, pharmaceutical industry, or healthcare.At least 3 years in a scientific or clinical management role.Demonstrated record of scientific contributions and publications in peer-reviewed journals.Solid understanding of clinical research methodologies and industry practices.Developing leadership abilities with experience managing scientific professionals.Strong communication and presentation skills.Analytical thinking and developing business awareness.Collaborative approach with strong interpersonal skills.Commitment to scientific integrity and ethical standards.Nice to Have
Experience in therapeutic areas aligned with the company\'s focus (e.g., CNS, oncology, neurology, rare diseases).Experience with digital health technologies, AI applications in clinical research, or innovative research methodologies.Experience in cross-functional project leadership.Background in clinical development or medical affairs.Understanding of regulatory requirements in clinical research.Language
Resumes must be submitted in English. Advanced level of English required.
Ready to join the adventure? Apply now and be a part of Signant Health\'s exciting journey.
Signant Health is proud to be an equal opportunity workplace and an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or veteran status.
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