Bristol-Myers Squibb Company

Engagement Strategy Lead

Location
Hopewell, NJ, United States
Posted
Apr 12, 2019
Ref
R1514828
Required Education
Bachelors Degree
Position Type
Full time
Summary

The Engagement Strategy Lead is a matrix leader with strong therapeutic area knowledge and portfolio expertise responsible for leading a team in the development of disease-specific recruitment strategy that focuses on creating a positive site and patient experience in BMS clinical trials. Additionally, the incumbent should have a keen interest in exploring, identifying and implementing innovative new approaches which support our clinical trial sites and patients. The Engagement Strategy Lead will have strong stakeholder management and communication skills and serves as the single point of accountability and contact for internal and external stakeholders for their assigned TA/indications. He/she will build relationships which support, raise awareness of and promote access to clinical trials in those areas.

Responsibilities

Responsible for leading a TA/indication focused matrix team in the development and implementation of a plan which appropriately utilize tactics including, but not limited to, connectivity with sites, patients/caregivers, and advocacy groups, enhanced digital capabilities, and/or other service offerings which optimize the site/patient experience and trial timelines.

Actively engages with multiple stakeholders throughout Global Clinical Operations (OPLs, Regional Leads, HUMs and CTP&AM colleagues) and the broader clinical trial team regarding disease-level strategies and site/patient insights; continuously communicates the benefit of tactics which support the engagement and recruitment plan.

Partners with enterprise colleagues on the development/maintenance of strong relationships with site and patient organizations to gain insight into their clinical trial experience and better inform our development and recruitment efforts. Collaborates with these organizations around awareness of and access to clinical trials and the drug development process.

Contributes to country and site planning by proactively bringing the "voice of the site/patient" into the process and ensuring that potential country-specific barriers to feasibility/recruitment/tactics are identified/communicated and mitigation strategies are considered and implemented, where needed/possible.

Partners with GCO Portfolio Leadership and BI&A to ensure awareness of portfolio priorities, operational timelines and issues are communicated to their assigned TA/indication team members. Contributes to the development of a cross asset plan as needed and accountable for its implementation by their matrix team.

Actively collaborates with enterprise site & patient facing teams (such as RCO, Global Advocacy, Multi-Channel Hub, HQ/US Medical, BMS Foundation, PBRGs) to ensure awareness of and alignment with ongoing activities. Partners on topics of mutual interest such as identification of new sites/networks, patient-focused drug development, alternate research models, diversity inclusion and planning, etc.

Actively drives innovation in clinical trials through awareness of external environment, focus on keeping patients and caregivers at the center while striving to be the site's preferred sponsor and through membership and/or engagement with internal efforts like Digital Acorn and external partnerships like Transcelerate Biopharma.

Partners with enterprise colleagues (multichannel hub, global procurement, etc.) to identify new opportunities which further enhance our engagement and/or recruitment toolkit. Contributes to the development of TA/indication specific digital health and innovation strategy.

Serves as a heavy contributor to the ongoing development, maintenance and enhancement of BMS Study Connect by seeking ways to leverage it as a communication platform to drive awareness of and access to BMS Clinical Trials.

Communicates a compelling vision of BMS clinical trials to outside organizations that generates respect and commitment to BMS as an industry leader in site and patient engagement efforts and functions as a subject matter expert on the drug development/clinical trial process.

Qualifications

BA/BS and/or MS degree with 8-10 years of pharmaceutical clinical development industry experience.

Demonstrated ability to manage complex projects with limited supervision and build strong relationships with internal and external partners.

Knowledge of the drug development process and the project management of clinical trials.

Proven ability to partner effectively with colleagues across multiple functions, geographies and at all levels of the enterprise.

Strong, proven stakeholder management and communication skills, particularly with senior leaders encouraged.

Position is based in Central New Jersey and involves limited travel.