Associate Scientific Director Clinical Development - Endocrinology

Recordati Industria Chimica e Farmaceutica S.p.A

$144K — $198K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • MD degree preferred or doctorate required with focus on endocrinology/metabolic diseases
  • Minimum of five years clinical experience required
  • Strongly preferred experience in endocrinology/metabolism clinical development
  • Pharmaceutical experience with knowledge of applicable regulations required
  • Proficient in Microsoft Office and tools for managing clinical trials

Responsibilities

  • Contribute to Clinical Development plan by identifying data gaps and proposing evidence generation strategies
  • Support clinical trial protocol development as a subject matter expert in endocrinology
  • Collaborate with clinical development and operations on clinical trial design and execution
  • Assist with regulatory interactions with the FDA and provide scientific justification for studies
  • Manage Investigator Sponsored Studies process and maintain communications with Principal Investigators
  • Provide scientific feedback to PIs on research outcomes and findings
  • Support overarching medical and clinical strategy and help develop scientific messages

Benefits

  • Health Insurance including medical, dental, vision, life & ADD, and disability insurance
  • Retirement benefits including 401k
  • Paid time off for vacation, holidays, and personal/sick leave
  • Company promotes a diverse environment and culture of inclusion
  • Opportunities for professional growth and significant impact on patient outcomes
Full Job Description
Reporting Structure

Reports To: Medical Director, Endocrinology, NA
Direct Reports: None
Areas Managed: North America (U.S. and Canada)

Overview

The Associate Scientific Director, Endocrinology, NA (North America) is a key role in the delivery and support of many of the scientific activities required to support RRD's Medical Strategy for the endocrinology franchise such as integrating Recordati's scientific and clinical data into programs supporting medical affairs. They help interpret and communicate scientific topics, ensuring that scientific integrity and medical insights guide all their activities. They are involved in delivering almost all aspects of externally facing medical communications and serve as subject matter expert for other roles in medical affairs (MA).

Essential Duties and Responsibilities

The Associate Scientific Director is directly responsible for delivering the following:
• Contributing to the Clinical Development plan, including identifying critical data gaps, defining evidence needs to support scientific objectives and key messages, and proposing data generation strategies that feed into the Scientific Data Evolution Plan.
• Supporting clinical trial protocol development as an endocrinology subject matter expert (SME), providing scientific and clinical guidance to ensure robust study design, methodological rigor, and alignment with clinical development objectives.
• Work collaboratively with evidence generation including clinical development and clinical operations on the design, execution, and interpretation of clinical trials in the endocrinology therapeutic area.
• Supporting clinical development regulatory interactions with the FDA, serving as the endocrinology SME providing scientific justification for study design, endpoints, and clinical rationale, and contributing to successful regulatory outcomes.
• Managing RRD's Investigator Sponsored Studies (ISS) process, including tracking received applications, managing the review process, tracking the contracting process and conducting ongoing scientific communications with funded Principal Investigators (PIs).
• Working with PIs that have completed their ISS to provide, at the PIs request, scientific feedback on their outcomes communications and ensure dissemination of clinically relevant findings across the RRD organization.
• Supporting the overarching endocrinology medical and clinical strategy such as situation analyses, identification of evidence needs, and development of key scientific messages to support Clinical Development and cross-functional alignment., all of which contribute to the tactical plans for the endocrinology franchise.

Education and Experience
• MD degree is required, with documented experience in endocrinology or metabolic diseases.
• Strong scientific background with at least five years of clinical experience.
• Endocrinology and/or metabolism clinical development experience is required.
• Pharmaceutical experience with a good knowledge of the applicable regulations is required.

Knowledge and Skills
• Proficiency in Microsoft Office suite, basic computer and typing skills, and tools/systems for managing clinical trials.
• Strong written and verbal English communication and presentation skills.
• Skilled at collaborating with stakeholders with varying viewpoints, influencing with and without authority, and negotiation. Includes relationship management of multiple stakeholders, internally and externally, such as KOLs, networks, PAGs (Patient Association Groups), CROs and others.

Work Environment

This job operates in a professional office environment. Based upon job requirements, employee may be required at times to attend meetings including travel out of province over weekends and nights. Employee must be able to freely operate and travel by car and train/plane modes of transportation. Employee is required to have a valid driver's license and passport.

Physical Demands

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. The employee must be able to fly via a commercial air carrier. This is largely a sedentary role when working in office; however, the employee frequently is required to stand; walk; use hands to finger, handle or feel; and reach with hands and arms; talk and hear. Occasionally is required to lift and/or move light to moderate weight up to 25 lbs.

Location/Travel
• This position is located at RRD HQ Office in Bridgewater, New Jersey with 3 days per week in the office as minimum expected.
• The position requires domestic travel (up to 30%); occasional international travel.

FLSA Classification
• This position is considered Exempt.

Disclaimer

This job description is not designed to cover or contain a comprehensive listing of the activities, duties or responsibilities that may be required.

Disclosures

Annualized Pay Range (Base Pay): $144,000 - $198,000
Other Types of Pay: Annual bonus Health Insurance: Medical, dental, orthodontia, vision, life & ADD, short and long term disability insurance benefits.
Retirement Benefits: 401k
Paid Time Off: Vacation, holiday, and sick/personal time.

At Recordati we believe in people! Inspired by our purpose - unlocking the full potential of life - we are committed to creating a diverse environment and cultivating a culture of inclusion. We strive to continually lead with our values and beliefs, enabling our employees to bring their whole selves to work and develop their potential.

If you are looking to join a company where you can try new things, speak openly, and be bold, we invite you to apply today.

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