Associate Medical Director, Clinical Development - Job ID: 1912, 1913, 1914 at Ascendis Pharma

Palo Alto, California, United States -

Full Time

Start Date

Immediate

Expiry Date

12 Sep, 26

Salary

265000.0

Posted On

14 Jun, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Trial Design, Medical Monitoring, Data Analysis, Regulatory Submissions, Clinical Development Planning, Endocrinology, Cross-functional Leadership, Scientific Inquiry, Medical Oversight, GCP, Patient Safety Monitoring, Stakeholder Management

Industry

Biotechnology Research

Description

Ascendis Pharma is a dynamic, fast-growing global biopharmaceutical company with locations in Denmark, Europe, and the United States. Today, we're advancing programs in Endocrinology Rare Disease and Oncology. Here at Ascendis, we pride ourselves on exceptional science, visionary leadership, and skilled and passionate colleagues. Guided by our core values of Patients, Science, and Passion, we use our TransCon® drug development platform to fulfill our mission of developing new and potentially best-in-class therapies to address unmet medical needs. Our culture fosters a place where skilled, adaptable, and highly resourceful professionals can truly make their mark. We offer a dynamic workplace for employees to grow and develop their skills. The Associate Medical Director is involved in the design, safety monitoring, and data analysis of the Company’s late-phase clinical trials in endocrinology. As such, the Associate Medical Director is an important and visible member of the clinical development team. The Associate Medical Director position is based in the United States, and will report to a Senior Medical Director, Clinical Development. Key Responsibilities Leverage medical expertise and hands-on clinical experience to promote relevance and rigor of the development program For clinical trials: design, provide medical oversight, and support site and subject retention Serve as a Medical Monitor for clinical trials, ensure study integrity, and track accumulating safety and efficacy data Provide leadership to study teams Ensure successful completion of trial-related documents (including clinical trial protocols, investigator brochures, medical monitoring plans, site training materials, clinical study reports, health authority responses, standard operating procedures, etc.) with cross-functional team members Anticipate obstacles within a clinical trial, and implement solutions Analyze, evaluate, interpret, and report study results Contribute to drafting and reviewing clinical documents, manuscripts, presentations, and regulatory submissions Contribute to design of the Clinical Development Plan Maintain up-to-date knowledge of relevant science, medical information, good clinical practices, and regulatory guidance Collaborate with—and serve as a clinical research resource for—cross-functional colleagues to optimize product development Cultivate relationships with investigative sites, clinical consultants, and key opinion leaders to represent the interests of the company Contribute to corporate strategic and organizational initiatives Assist with commercial activities as needed Complete assigned tasks thoroughly, accurately, and on time Adhere to rigorous ethical standards Travel up to 20% domestically and internationally for scientific meetings Knowledge, Skills and Experience M.D. degree Completion of ACGME-accredited residency and fellowship (strongly preferred) Physician licensure in at least one state (strongly preferred) Board-certified (strongly preferred), with specialty in endocrinology highly desired At least 3 years of industry (other relevant experience e.g. post-graduate experience in the clinical and/or academic realms may also be considered on a case-by-case basis). At least 2 years of experience with clinical trial design and execution Strong track record of scientific and clinical inquiry Possess excellent communication skills (written and oral) Learn quickly, follow complex directions under pressure Multi-task while remaining organized and attentive to detail Lead both directly and by example Work hard, be a trustworthy and collaborative team player Take initiative and solve complex problems Demonstrate sound judgement in terms of handling complex, confidential, and regulated information The estimated salary range for this position is $255-265K/year. Actual salary determination is dependent on a variety of factors some of which include: experience, qualifications, and geographic location. This position may be eligible for a discretionary annual bonus or an incentive compensation plan (eligibility varies based on role and position level), discretionary stock-based long-term incentives, paid time off, and a comprehensive benefits package. 401(k) plan with company match Medical, dental, and vision plans Company-offered Life and Accidental Death & Dismemberment (AD&D) insurance Company-provided short and long-term disability benefits Unique offerings of Pet Insurance and Legal Insurance Employee Assistance Program Employee Discounts Professional Development Health Saving Account (HSA) Flexible Spending Accounts Various incentive compensation plans Accident, Critical Illness, and Hospital Indemnity Insurance Mental Health resources Paid leave benefits for new parents A note to recruiters: We do not allow external search party solicitation. Presentation of candidates without written permission from the Ascendis Pharma Inc Human Resources team (specifically from: Talent Acquisition Partner or Human Resources Director) is not allowed. If this occurs your ownership of these candidates will not be acknowledged.

Responsibilities

The Associate Medical Director oversees the design, safety monitoring, and data analysis of late-phase clinical trials in endocrinology. They serve as a Medical Monitor and lead cross-functional teams to ensure the successful completion of trial-related regulatory documents.