Senior Director, Scientific and Clinical Programs
Company: National Multiple Sclerosis Society
Location: Philadelphia
Posted on: November 14, 2024
Job Description:
WHO WE ARE:The National Multiple Sclerosis Society mobilizes
people and resources to drive research for a cure and to address
the challenges of everyone affected by MS. To fulfill this mission,
the Society funds cutting-edge research, drives change through
advocacy, facilitates professional education, collaborates with MS
organizations around the world, and provides programs and services
designed to help people with MS and their families move their lives
forward. We partner with volunteers to accomplish our work. Staff
members engage volunteers through effective and timely
communications, facilitating meaningful opportunities, and
continually seeking and providing feedback for reciprocal growth
and learning.This position will lead the development and
implementation of the International Advisory Committee on Clinical
Trials in MS (CTC) scientific and communication strategies
(https://ectrims.eu/ms-clinical-trials-committee/). The individual
will be responsible for providing day-to-day leadership for ongoing
CTC global initiatives and developing new programs. They will have
a critical leadership role in ensuring the confidence, engagement,
participation of leadership/general members of the CTC and the
global scientific and health care provider community.
The mission of the International Advisory Committee on Clinical
Trials in Multiple Sclerosis is to provide perspective and guidance
to the multiple sclerosis (MS) scientific and health care provider
community related to planning and implementation of clinical trials
of MS therapies and related topics. The committee consists of 35-40
global leaders in MS clinical and translational research and is
well known for the development of McDonald Diagnostic Criteria for
MS, the MS clinical course descriptors, clinical trial design
methodologies, and guidance regarding the treatment of MS.
The CTC convenes international meetings and consensus-building
activities on specific topics determined to be high priority by
Committee leadership. Outcomes of these activities are typically
published in high-impact scientific journals as well as channels
accessible by the public. This CTC is a global body sponsored by
the European Committee for Treatment and Research in MS (ECTRIMS)
and the National MS Society. The incumbent would be an employee of
the Society and have accountability to both the sponsors.
The incumbent will serve as an intellectual and analytical leader
for CTC and project manage a number of high-profile activities in
parallel. They will regularly engage and interact with committee
chairs, committee members and scientific thought leaders to shape
the CTC research and clinical strategy as well as communicate
research advances to Society and ECTRIMS constituents, donors, and
the public. This person represents the Society and CTC at external
convening activities, advances CTC initiatives, and cultivates
relationships and collaboration opportunities to leverage resources
with like-minded organizations and funding partners.Essential
Functions / Responsibility SCIENTIFIC AND CLINICAL PROGRAM
MANAGEMENT & LEADERSHIP (CTC): Working with Society and ECTRIMS
scientific and operational staff, the individual will provide
leadership for CTC strategic research and clinical initiatives.
- Drive the overall multi-year strategy for CTC committee in
partnership with Society and ECTRIMS leadership
- Develop comprehensive project plans aligned with CTC scientific
and clinical strategies and priorities to implement, communicate
and implement multiple projects, track progress and performance, to
be shared with CTC leadership, staff and committee members
- Working with CTC leadership, engage the international academic,
clinical and commercial research community to develop innovative
solutions and consensus around for MS challenges and
opportunities
- Lead and manage the coordination, alignment, changes in project
scopes and budgets to fulfill partnership and collaborative work
with ECTRIMS for the Clinical Trials Committee
- Manage the CTC Sponsor group (the board of the CTC) including
organizing quarterly meetings, drafting annual reviews, and
ensuring timely financial planning and reporting
- Measure project performance against milestones and deliverables
using appropriate tools and techniques
- Will have autonomy to make key decisions, but will report and
escalate potential challenges and opportunities to EVP, Research,
as needed
- Will report to CTC leadership, committees and staff as
necessary; Liaise with the EVP, Research and the Director, Global
Initiatives; Liaise with Society Research, Advocacy, Healthcare
Access and Global Strategy departments to assure alignment and
maximize on collaboration opportunities
- Create, receive, maintain and archive comprehensive project
documentation to provide a history of the projects for use in
similar projects in the future
- Identify and assess risks and develop plan of action if
problems arise.
- Manage the development and project growth of new scientific or
clinical initiatives within the CTC
- Perform other related duties as assignedMEETING PLANNING AND
CONTENT DEVELOPMENT (CTC): Lead Scientific meeting planning,
content development and support for CTC in person and virtual
meetings
- Organize oversight and planning meetings (teleconference and
in-person) for ongoing CTC initiatives. Develop agendas, slide
decks and meeting tools to share data and reports
- Develop and organize scientific meetings focused on CTC
research portfolio and strategic initiatives. Assist with
development of program and agendas and secure speakers for Alliance
scientific strategy meetings
- Conduct program assessments and portfolio analysis for CTC
leadership
- Prepare scientific reports and presentations for CTC leadership
and committee members
- Drive and facilitate writing of scientific and consensus papers
for publishing in key scientific journalsScientific Program
Management: Provide Scientific Program Management to Society
Research projects.
- Manage review processes for Society Research Awards
- Direct a portfolio of scientific initiatives of the
Society
- Develop comprehensive project plans aligned with Society
scientific strategies to monitor multiple projects and track
progress and performance to be shared with Society staff and
volunteers
- Manage changes to the project scope, project schedule and
project costs using appropriate verification techniques
- Measure project performance against milestones and deliverables
using appropriate tools and techniques
- Report and escalate potential issues and opportunities to EVP,
Research, as needed
- Create, receive, maintain and archive comprehensive project
documentation to provide a history of the projects for use in
similar projects in the future
- Accurately estimate budgets and monitor the actual spend as
compared to the planned budget. Report and adjust accordingly.
- Identify and assess risks and develop plan of action if
problems arise.
- Manage the development and project growth of new scientific
initiatives within the Society
- Manage award agreement changes when needed (and identify
critical issues and promptly inform and propose mitigation
actions)
- Perform other related duties as assignedRole
Qualifications:Education:
- PhD/MD/DO/NP/PA or other comparable post-graduate degree with
7-10 years of research or clinical experience and 3-5 years
experience conducting and managing research in the biotechnology or
pharmaceutical sector and/or clinical care or nursing - preferably
in MS. Experience in patient advocacy/non-profit setting is
preferred. Demonstrated track record of supervising staff and
managing multidisciplinary teams in a matrix
environment.Experience:Scientific Project Management,
Communication, Planning, Managing and Measuring Work, Negotiating,
Diplomacy, Analysis, Managing Systems, Managing Processes, Active
Listening, Building RelationshipsKnowledge and Skills:
- High level planning, program and project management skills to
ensure effective use of resources (Essential)
- Vision, strategic insight and intellectual capability to
understand the environment in which the CTC is operating, and to
develop/refine the strategy accordingly (Essential)
- Outstanding leadership skills with ability to adapt style to
circumstances (Essential)
- Ability to focus on impact and deliver outstanding results in a
team environment and contribute positively as part of a team
(Essential)
- Exceptional interpersonal skills, able to influence a wide
range of stakeholders (Essential)
- Communications - excellent written and verbal skills in English
(Essential)
- Ability to cope with, and resolve, conflict.
- Ability to manage and deliver a complex and diverse
workload.
- Results oriented, takes initiative and ownership to get the job
done
- Experience supporting large, geographically dispersed projects
in the voluntary, public sector or multi-site environment of
comparable size and complexity, to deliver high quality results to
deadlines and under pressure (Preferred) Competencies/Behaviors:
- Able to take a strategic overview and work collaboratively and
effectively with international teams and senior management to drive
strategic goals
- Emotionally resilient and able to work with ambiguity, group
pressures, the opposition of ideas and difficult tasks
- Able to work under pressure and adapt to change
- Willingness to have flexibility to work outside of 'normal'
office hours regularly (due to the worldwide CTC membership)
- Approachable - Will be open minded and value diversity
- Empowering - will enable positive change
- Passionate about the Society and CTC's goals and delivering
excellenceTechnical Competencies:Financial Management
- Work with the Executive Vice President, Research and finance to
ensure the efficient management of Alliance expenditures, including
effective budget preparation, planning and monitoring for the
CTCGeneral
- Some domestic and international travel will be required
- Experience and proficiency with computer software such as
Microsoft Office, MS Project, particularly database use,
spreadsheet and analytical software, or willingness and ability to
rapidly gain such expertise, is required for this position.
Understanding the administrative and operational aspects of medical
research in a clinical setting is required; prior exposure to
issues relevant to MS highly desirable.
- Ensure compliance with the CTC's policies including: The
perspective of people affected by progressive MS as a critical
component of decision-making; all meetings and activities are
conducted with accessibility in mind; data and information is
shared; collaboration across organizations and borders is
paramount; transparency in decision-making is a discipline
- Ensure compliance with the Society's policies on working with
people with MS, Volunteers, Recruiting Safely, Safeguarding, Health
& Safety and Equality & Diversity
- Ensure compliance with the Society's guidelines on the
requirements of DisclosureCompensation & Benefits Info:Estimated
hiring compensation range for this role is $96,000 - $135,000 based
on our average compensation schedule.Final offers will be based on
candidategeographic location and consider career experience and may
vary from this range due to these and other factors.The National
Multiple Sclerosis Society provides a highly competitive,
comprehensive benefit package to employees. These benefits include
a considerable Paid Time Off Plan; Paid Holidays; 401k Retirement
Savings Plan with Society match; Educational Reimbursement Plan;
Professional Development Assistance; Commuter Benefit Plan;
Comprehensive Health & Welfare benefits including Medical, Dental,
Vision, Flex Spending Accounts, Life Insurance, Disability
Coverage, Life Assistance Plan as well as additional voluntary
benefit offerings.The Society has a career framework that is our
foundation of a clear, consistent structure for growth and careers.
It is comprised of career bands and career levels, as well as
functions and disciplines, that together, capture the Society's
positions and work. This position is in the Professional career
band and a level of 5 (P5).The National MS Society is committed to
building a diverse and inclusive workforce. We strive to create a
workforce that reflects the communities we serve and where everyone
feels empowered to bring their authentic selves to work. We need
you and your unique talents and perspectives to help us write the
last chapter on MS.APPLICATION INSTRUCTIONS:We appreciate your
consideration of our job opportunities and strive to make it as
effortless as possible to apply for our positions. With only a few
required sections and the option to use our resume parsing tool, we
aim to streamline the application experience, saving you time and
effort. Additionally, if you wish to include a cover letter with
your application, please feel free to attach it along with your
resume, and any other documents required, to the Resume/CV document
upload section at the bottom of the My Experience page. We
appreciate your interest in joining our team and look forward to
receiving your application!Important: Please check the job posting
to see if a Cover Letter or any other documents are required for
the position you are applying to. You will not be able to modify
your application after you submit it. The My Experience page is the
only opportunity to add your cover letter and supporting document
attachments. If you experience any trouble submitting your
materials, please check out our .
Keywords: National Multiple Sclerosis Society, Wilmington , Senior Director, Scientific and Clinical Programs, Accounting, Auditing , Philadelphia, Delaware
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