Associate* Clinical Development Director - Cardiovascular

Healthcare Businesswomen’s Association; Ontario; On-site; CAD 100,000 - 140,000; Full time

Job summary

A global healthcare company seeks an Associate Clinical Development Director in Canada to lead clinical development initiatives. The successful candidate will have significant experience in clinical research, a strong life sciences background, and the ability to effectively guide cross-functional teams in a dynamic environment. This role is pivotal in ensuring clinical deliverables meet regulatory and scientific standards.

Qualifications

• Minimum > 3 years (Associate) or 7 years (CDD) in clinical research or drug development.
• Demonstrated ability to establish effective working relationships with key investigators.
• Strong communication skills in a cross-functional global organization.

Responsibilities

• Providing clinical leadership and strategic input for all clinical deliverables.
• Driving execution of the clinical program in partnership with global line functions.
• Overseeing medical and scientific review of clinical trial data.

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 preferred

Job description

Job Description Summary

The Associate* Clinical Development Director (CDD) in the Cardio Renal & Metabolic (CRM) Development Unit is responsible for leading the strategic planning and management of the assigned clinical program(s) from an end-to-end clinical development perspective. As a CDD in the CV TA, you will have oversight of the clinical development for the assigned programs and drive the execution of the clinical development plan. In addition, you will enable an empowered organization, which can navigate in a matrix environment and adjust quickly to business needs.

Job Description

Major accountabilities:

• Providing clinical leadership and strategic input for all clinical deliverables in the assigned project or section of a clinical program. Clinical deliverables may include clinical sections of individual protocols or sub studies consistent with the Integrated Development Plans (IDP), clinical data review, program specific standards, clinical components of regulatory documents/registration dossiers, and publications
• Leading development of clinical sections of trial and program level regulatory documents
• Driving execution of the section of the clinical program in partnership with global line functions, assigned Global Trial Directors (GTDs), and regional/country medical associates, if applicable
• Overseeing/conducting ongoing medical and scientific review of clinical trial data with Clinical Scientific Expert(s) with appropriate oversight from Medical Lead
• Supporting (Sr.) GPCH in ensuring overall safety of the molecule for the assigned section and may be a core member of the Safety Management Team, supporting overall program safety reporting in collaboration with Patient Safety
• As a clinical expert, supporting the (Sr.) GPCH or CDH in interactions with external and internal stakeholders and decision boards
• Contributing to scientific training of relevant Novartis stakeholders on the disease area and compound/molecule. May serve as speaker for franchise medical/scientific training and may be the Program Manager of other associates

Minimum Requirements:

• Advanced degree in life sciences / healthcare (or clinically relevant degree) is required. PharmD or PhD is strongly preferred***
• Minimum > 3 years (Associate) or 7 years experience (CDD) in clinical research or drug development
• Working knowledge of the assigned disease area is desired with proven ability to interpret, discuss and present efficacy and safety data relating to clinical trial(s) or program level
• Demonstrated ability to establish effective working relationship with key investigators
• Working knowledge of GCP, clinical trial design, statistics, and regulatory and clinical development processes
• Strong communication skills with the ability to work in a cross functional and global organization

* Final job title (Associate Clinical Development Director, Level 5/ Clinical Development Director, Level 6 and associated responsibilities will be commensurate with the successful candidates’ level of expertise.

Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture

You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards

Commitment to Diversity and Inclusion:

Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.

Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here:

https://talentnetwork.novartis.com/network

Skills Desired

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