Associate Clinical Development Director in London

LOCATION: London, Dublin, Barcelona

ROLE TYPE: Hybrid Working, #LI-Hybrid

The Associate Clinical Development Director (Assoc. CDD) provides input to the development of protocols for assigned global clinical trials, scientific monitoring, and reporting of quality data. May be assigned to provide support to the development of the clinical and scientific strategy of assigned sections of a clinical development program, depending on the size and complexity.

Major accountabilities:

• Provides input to the development of clinical development strategy, and contributes to the development of trial related documents (e.g., CTPs, informed consent form, case report forms, data monitoring committee charters, data analysis plan, reports, publications) for assigned clinical trial(s) consistent with Clinical Development Plan (CDP); develops materials for trial-related advisory boards, data monitoring committees, investigator meetings, and protocol training meetings for Novartis local clinical development teams.
• Provides clinical and scientific input and contributes to clinical sections of trial and program level regulatory documents (e.g., Investigator’s Brochures, Health Authority briefing books, safety updates, submission dossiers, and responses to Health Authorities).
• In collaboration with appropriate Clinical Trial Team (CTT) members: Ensures clinical development oversight and support of trials as needed; conducts ongoing scientific review of clinical trial data with Clinical Scientific Expert(s) with appropriate oversight from Medical Lead/CDMD/CSL.
• Manages patient safety reports on trial data to safety and clinical boards (e.g., Safety Management Team (SMT), GCT, GPT) with appropriate oversight from Medical Lead/CDMD/CSL in collaboration with patient safety.
• Provides input into final analyses and interpretation including the development of the Clinical Study Report(s) (CSRs), publications and internal/external presentations, with appropriate oversight from Medical Lead/CDMD/CSL.
• Contributes to global initiatives (e.g., process improvement, training, SOP development, other Clinical Development line function initiatives).
• May be assigned to lead clinical trial(s) as Clinical Scientific Lead and provide leadership and guidance for all clinical aspects of a clinical trial in close collaboration with the assigned medical monitor and/or CDMD.

Education:

Advanced degree in life sciences/healthcare (or clinically relevant degree) is required. PharmD, or PhD strongly preferred.

Languages: Fluent oral and written English.

Experience/Professional requirement:

• ≥ 3 years of involvement in clinical research or drug development in an academic or industry environment spanning clinical activities in Phases I through IV.
• ≥ 2 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 the pharmaceutical industry.
• 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 relationships with stakeholders.
• Working knowledge of ICH, GCP, clinical trial design and methodology, statistics, and regulatory and clinical development processes.
• Strong communication skills, written and oral.
• Strong interpersonal skills.
• Strong negotiation and conflict resolution skills.
• People management preferred.

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.

#LI-hybrid

Skills Desired: Budget Management, Clinical Research, Clinical Trial Protocol, Clinical Trials, Coaching, Data Analysis, Data Integrity, Learning Design, Lifesciences, Risk Monitoring, Trends Analysis.