Senior Clinical Development Director - Renal

Legend Biotech USA; East Hanover (NJ); On-site; USD 204,000 - 380,000; Full time

Job summary

An established industry player is seeking a Senior Clinical Development Director to lead clinical programs and trials. This pivotal role involves driving clinical deliverables, collaborating with global teams, and ensuring data quality and compliance with regulatory standards. The ideal candidate will have extensive experience in clinical research, strong scientific acumen, and a proven track record in managing complex clinical trials. Join a forward-thinking company dedicated to innovation and excellence in healthcare, where your contributions will significantly impact patient outcomes and drug development processes.

Benefits

401(k) eligibility

Paid time off benefits

Medical benefits

Discretionary awards

Restricted stock units

Sign-on bonus

Qualifications

• 10+ years in clinical research and drug development.
• Experience in Phases I through IV clinical trials.
• Solid scientific writing and regulatory submission skills.

Responsibilities

• Lead clinical deliverables and strategy for assigned programs.
• Collaborate with cross-functional teams for data quality.
• Support safety reporting and regulatory documentation.

Skills

Budget Management

Clinical Research

Clinical Trials

Coaching

Cross-Functional Teams

Lifesciences

People Management

Risk Management

Risk Monitoring

Education

Advanced degree in life sciences/healthcare

PharmD or PhD

Job description

Job Description Summary
The Senior/Clinical Development Director (Sr*CDD) is the clinical/scientific expert and if assigned the clinical development lead of a section of a global clinical program and/or trial. (e.g., an indication, a new formulation, or a specific development phase) or a large, complex trial, under the leadership of the GPCH. The Sr* CDD may be assigned to have a team leadership role for sections clinical programs and/or global clinical trials, depending on the size, nature and complexity

Job Description

Major accountabilities:

• Supports and if assigned leads delivery of all assigned clinical deliverables in the assigned section of a clinical program. Clinical deliverables may include the clinical development strategy for assigned program section(s), clinical sections of individual protocols consistent with the Integrated Development Plans (IDP), clinical data review program specific standards, clinical components of regulatory documents/registration dossiers, and publications
• Contributes and if assigned leads development and delivery of clinical sections of trial and program level regulatory documents (e.g., Investigators Brochures, briefing books, safety updates, submission dossiers, and responses to Health Authorities)
• Drives execution of the section of the clinical program in partnership with global line functions, in particular clinical operations, trial leaders and data management/analysis, and regional/country clinical development associates
• Ensures ongoing clinical and scientific review of clinical trial data.
• Work in close collaboration with the data management and statistics teams to ensure proper data quality and analysis of clinical trial results.
• May be the Program or Function Manager of associates (e.g., CDD or associate CDD
• Supports GPCH in assessing overall risk-benefit of the molecule for the assigned section of the clinical program, may be a (core) member of the Safety Management Team (SMT), and supports overall program safety reporting (e.g., Periodic Safety Update Reports (PSURs), Drug Safety Update Reports (DSURs), and other safety related documents) in collaboration with the medical monitor, CDMD and Patient Safety
• Member and if assigned may (co-)lead the Global Clinical Team (GCT), if there is a separate GCT for the assigned program section. Represents the section when assigned in Global Program Team (GPT) meetings, and as the section spokesperson in internal and external meetings/boards, as assigned
• Supports the Clinical Development Head (CDH) by providing clinical/scientific input into IDP/CDP and CTP reviews and contributing/driving development of disease clinical standards for new disease areas. May take on other TA responsibilities as directed by the CDH

Minimum Requirements:
Work Experience:

• Advanced degree in life sciences/healthcare (or clinically relevant degree) is required. PharmD, or PhD strongly preferred
• ≥ 10 years of involvement in clinical research, global drug development in an academic or industry environment spanning clinical activities in Phases I through IV. ≥ 5 years of contribution to and accomplishment in all aspects of conducting clinical trials (e.g., planning, executing, reporting and publishing) in a global/matrix environment in pharmaceutical industry. Experience in late phase clinical development strongly preferred
• Solid scientific writing skills
• Experience with regulatory submissions (IND, NDA/BLA, CTA/MAA) preferred
• Solid and advanced scientific acumen and ability to analyze and interpret scientific literature and data. Strong affinity with data, data quality and analysis.
• Preferred knowledge and/or experience of assigned therapeutic area
• Demonstrated ability to establish strong scientific partnership with key internal and external stakeholders
• ≥ 3 years people management experience required; this may include management in a matrix environment*

Final job title Senior Clinical Development Director, Level 6 / Clinical Development Director, Level 6 and associated responsibilities will be commensurate with the successful candidates level of expertise.

Novartis Compensation and Benefit Summary: The pay range for this position at commencement of employment is expected to be between: $204,400 and $379,600/year; however, while salary ranges are effective from 1/1/25 through 12/31/25, fluctuations in the job market may necessitate adjustments to pay ranges during this period. Further, final pay determinations will depend on various factors, including, but not limited to geographical location, experience level, knowledge, skills, and abilities. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an at-will position and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.

Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

EEO Statement:

The Novartis Group of Companies are Equal Opportunity Employers who are focused on building and advancing a culture of inclusion that values and celebrates individual differences, uniqueness, backgrounds and perspectives. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We are committed to fostering a diverse and inclusive workplace that reflects the world around us and connects us to the patients, customers and communities we serve.

Accessibility and reasonable accommodations

The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to [e-mail] or call [phone] and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

Salary Range
$204,400.00 - $379,600.00

Skills Desired
Budget Management, Clinical Research, Clinical Trials, Coaching, Cross-Functional Teams, Lifesciences, People Management, Risk Management, Risk Monitoring