Associate Director Clinical

Senior Recruiter | Championing Diversity & Hiring Excellence

Want to do the Best Work of Your Life?

Working at Signant Health puts you at the very heart of the world’s most exciting sector - a high-growth, dynamic company in an extraordinary industry. We’re radically changing the clinical trial landscape, driving change through the technology and innovations we create and the services we deliver to our customers.

Where do you fit in?

The Associate Director Clinical supports strategic initiatives within the Science and Medicine department and DHS group, contributing to the alignment of scientific activities with business objectives and corporate growth strategies. The Associate Director is responsible for supporting the Science and Medicine leadership team in implementing scientific initiatives and key departmental projects. The Associate Director contributes to thought leadership, ensures scientific quality, and represents the company as a scientific expert in selected forums.

As part of our team, your main responsibilities will be :

• Support strategic initiatives for the Science and Medicine department and DHS group, contributing to the alignment of scientific activities with business objectives and corporate goals. Play a critical role in accelerating business development by collaborating closely 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 a culture of 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 provide review of methodologies and deliverables.
• Represent the company at selected Investigator’s meetings, scientific conferences, industry meetings, and with stakeholders, serving 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 compliance with regulatory requirements and industry standards while maintaining scientific integrity across projects.

Decision making and influence :

You’ll need to bring :

Does this sound like something you’d like to explore? Then we’d love to hear from you!

Please apply below. We review and respond to every application, keep an eye on your inbox for our reply.

Please note that Signant does not accept unsolicited resumes from Third Party vendors.

Job details

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