Vice President/Senior Vice President, Clinical Development

Tbwa Chiat Day Inc
US - Massachusetts - Waltham
November 4, 2024

Vice President/Senior Vice President, Clinical Development Waltham, Massachusetts
At Kailera, we are bold, authentic and committed to our mission of developing therapies that give people the power to transform their lives and elevate their overall health.
Rooted in an entrepreneurial spirit and a team-oriented culture, we are working together to advance Kailera's mission to advance novel therapies for obesity and related conditions.
We are passionate about creating an inclusive workplace that promotes collaboration, integrity, and excellence.
As we expand, we seek the most talented individuals with diverse backgrounds, cultures, perspectives, and experiences to join our team.
What You'll Do:

This is a critical leadership role within the medical organization.
The Head of Clinical Development leads the development and execution of the global medical and scientific evidence generation strategy for our products.
They solicit and incorporate cross-functional input into this strategy, translate it into an aligned vision and actionable global development plan, and are accountable for its execution.
They develop key external scientific relationships with leaders in the obesity research community and interact with global regulatory authorities.
Responsibilities:

Build, grow, and lead the global clinical development organization
Develop and execute global development strategy and resultant evidence generation plan with incorporation of cross-functional and regional input
Design, execute, complete, and communicate clinical trials (eg, scientific advisory boards, protocol development, regulatory and ethic committee interactions, medical monitoring, data analyses, study reports, regulatory correspondences and filings, presentations, and data dissemination)
Deliver robust clinical trial data on-time and on-budget to inform product benefit:
risk
Interface with global medical opinion leaders in obesity to inform clinical development program and maintain engagement
Clear, data-based communications with global regulators
Provide clinical input to regulatory, safety, medical affairs, commercial, payer, and manufacturing colleagues
Qualifications:

MD or equivalent
At least 15 years of clinical development experience with proven track record of executing clinical trials and global regulatory interactions
Experience in obesity and/or metabolic disease strongly preferred
Prior leadership, budgeting and resource management experience required
Uncompromising ethics, passion for teamwork and people, attention to detail, solution focus, and strong communication skills
Ability and willingness to fly at necessary altitude to get job done
A drive for problem solving, continual learning, and attracting, mentoring, and retaining best people
At Kailera, we are committed to fostering an inclusive culture.
How we treat our people is reflective of this commitment.
We share the pay range for this particular role with the actual base salary depending upon factors such as job-related knowledge, skills, market factors, and experience.
Salary Range:

$245,000 - $320,000 USD
EQUAL EMPLOYMENT OPPORTUNITY INFORMATION:

Kailera Therapeutics, Inc.
is an Equal Opportunity Employer that does not discriminate on the basis of actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender, gender identity or expression, sexual orientation, marital status, military service and veteran status, physical or mental disability, genetic information, reproductive health decisions, domestic victim status, political affiliation, or any other characteristic protected by applicable federal, state, or local laws and ordinances.
E-Verify:

uses E-Verify to confirm the identity and employment eligibility of all new hires.
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Read the full job description and apply online on the recuiter's web-site

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