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Associate Director Ecosystem (Clinical Study Management)
116185
Posted:
15th
March 2023
- 150000 USD - 175000 USD
- Chicago, United States
- Permanent
Associate Director Ecosystem (Clinical Study Management)
Are you looking to join a top 5 Global Biopharma?
Do you have a passion for challenging the efficacy and technology used within Clinical Trials?
Are you driven to make change and strive for better advancement in technology capabilities?
If so, please read on, I am partnered with a Top 5 Global Biopharma, who are looking to add an Associate Director to there Ecosystem Enablement division with a focus on the Clinical Study Management technology. This role will continue to advance and challenge the ecosystem of the technology used within their clinical trials, whilst management stakeholder expectations to ensure both the business unit and the Clinical study unit's technologies are working to the best efficiency's.
Responsibilities
- Promotes ecosystem approach and develops CDO Sr. Aligning the leadership and BTS to guarantee that the organisation conducting clinical trials has the proper support.
- Develop crucial SME connections and networks within CDO divisions to get clinical teams' feedback on technology needs
- Assume leadership responsibility for all ecosystem project deliverables, including budget planning, change management, release schedule management, development prioritisation, and strategic decision-making. Assure timely and cost-effective implementation.
- Do an impact evaluation to evaluate the efficiency of recently introduced and current technology
- Establish and maintain an ecosystem roadmap, assess all systems annually, and identify possibilities for decommissioning, improving current systems, or both.
- In order to transform business processes, project manage technical implementation initiatives, improvements, and/or deliverables, such as the rollout of cross-functional systems and upcoming system releases and enhancements.
Skills required
- Appropriate education, experience, or work-related training in the biological sciences or healthcare.
- 6 years of experience in the pharmaceutical industry with expertise in project management or business technology support and knowledge of clinical trials, clinical trials procedure, and technology.
- Working in a matrixed workplace with project management experience. System usage in clinical trials experience is preferred.
- Effective communication abilities were on display. demonstrated aptitude for explaining abstract and technical ideas to non-technical audiences
- Demonstrated aptitude for analysis and problem-solving. a track record of effectively managing many priorities and carrying out tasks in a fast-paced workplace.
Location: Illinois, USA
I am looking for individuals who are looking to embark on a fabulous career path with this Top 5 Global Biopharma, with interviews happening immediately, please do reach out to discuss.
Contact Ryan at Meet on +1 (646) 582-3768 or email me at ryan.tanner@peoplewithchemistry.com