CLINICAL DEVELOPMENT LEAD - CAMBRIDGE - MA
Company: National Guard Employment Network
Location: Cambridge
Posted on: August 28, 2024
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Job Description:
Job Description
ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works
with partner companies to source qualified talent for their open
roles. The following position is available to Veterans,
Transitioning Military, National Guard and Reserve Members,
Military Spouses, Wounded Warriors, and their Caregivers. If you
have the required skill set, education requirements, and
experience, please click the submit button and follow the next
steps. Unless specifically stated otherwise, this role is On-Site
at the location detailed in the job post.
Clinical Development Lead - Neuroscience/Psychiatry
Position Summary
CDLs are matrix leaders and managers who lead, develop, motivate
and achieve results through teams; demonstrate a commitment to the
development of a resilient attitude, embrace change and have an
unwavering commitment to our People Strategy
Serves as the clinical point of accountability for the Development
Team and is responsible for navigating the overall clinical
development plan for complex programs that have a large impact on
the business. Ensures clinical studies are aligned with target
label indications and are designed to meet regulatory, quality,
medical, and access goals
Serves as a matrix leader to lead, develop, motivate and achieve
results through teams, and is the direct manager to Clinical Trial
Physicians (CTPs)
Position Responsibilities
Accountable for the clinical contribution to the development of
each indication strategy, including registrational and
non-registrational studies, with the support of the CTPs and
Clinical Scientists (CS) within the asset and/or indication
Responsible for managing clinical trial physician(s); attracting,
developing and retaining top talent; ensuring appropriate training
and mentoring of clinical trial physicians
May serve as CTP as necessary
Accountable in partnership with the Clinical Scientist and
Statistician for the design, execution, and analyses of each study
led by the CTPs and CSs. Should work to proactively partner with
these roles
Accountable for clinical content for CSRs, regulatory reports,
briefing books, submission documents, and periodic updadates
Champions a quality-focused mindset and ensures adherence to GCP
and compliance obligations for clinical conduct
Represents Clinical Development in both internal and external
forums as the consulted authority for the disease area, including
within Business Development function
Partners with Worldwide Patient Safety physicians in the ongoing
review of safety data
Serves as the (co-)leader of the cross-functional Clinical
Development Team
Provides clinical leadership and disease area expertise into
integrated disease area strategies
Partners closely with KOLs, to seek input into the design,
execution, analysis and reporting of studies.
Serves as Primary Clinical Representative in Regulatory
interactions
Evaluates strategic options against a given Target Product Profile
(TPP)
Collaborates with Global Development Operations/Global Compliance
Group to develop asset level risk management plan, resolves issues
with Quality/CS, and raises to DT as needed
Sets executional priorities and partners with CTP and CS to support
executional delivery of studies
Accountable for top line data with support of CTP, CS, and
Statisticians
Other clinical development responsibilities as assigned by Head of
Late Development for Neuroscience
Experience Requirements
The Senior Director CDL has demonstrated leadership in the design
and execution of multiple clinical trials having had significant
experience as a senior clinical leader and exhibits all of the
following attributes:
Able to synthesize internal and external data to produce a clinical
strategy.
Demonstrated success in formulating clinical development strategy
across increasingly complex clinical programs with large impact on
the business.
Able to ensure that the clinical program will result in a viable
registrational strategy
Demonstrated success in designing and executing multiple clinical
trials, with significant experience as a clinical leader.
Has achieved the knowledge base to serve as a a trusted internal
expert in the therapeutic area, asset, indication, and clinical
development, and is viewed as a peer by external academic
collaborators and other KOLs.
Able to assess personnel needs, translate into a hiring strategy,
and lead the hiring efforts
Able to work with other stakeholders to ensure a robust enterprise
level strategy for asset(s) and indication(s) including early, late
and post-marketing development, as well as awareness of the
enterprise disease area portfolio
CDL has demonstrated sustained excellent performance as Clinical
Trial Physician, Clinical Scientist, or equivalent
Verifiable track record of successful people management and
development or leadership in a matrix team (e.g. mentoring junior
colleagues)
Interface across multiple functions to mediate conflict resolution,
and champion an organizational culture to promote behaviors that
lead to meaningful synergies and superior performance.
In addition, the CDL should have all the following experiences and
capabilities:
Expertise in implementing scientific methods to test hypotheses,
design, analyze, interpret and report results
Ability to recognize, articulate, and accept calculated risks to
make informed decisions
Deep understanding of the fundamentals of protocol development and
follow up, including but not limited to study monitoring, data
collection and analysis, database cleaning and database lock
Understanding of pharmacokinetics, biomarkers, statistical
principles, and regulatory requirements
Comfortable working in a fast-paced environment; ability to support
multiple, complex, studies in parallel
Willing to work outside of a traditional functional environment, in
a team unified around serving the assets
Willingness and ability to form strong, productive partnerships
with external providers/thought leaders
Possess excellent communication skills and experience delivering
effective presentations on both technical and non-technical
subjects.
Key Competency Requirements
CDL has demonstrated excellent skills in clinical development
strategy including the clinical components of regulatory
submission(s)
External focus to understand the trends in the disease area
treatment paradigms and ability to build relationships with
external partners, thought leaders and collaborators outside of
BMS
Partner and interact with colleagues from Early Development who
design and implement first in human through proof-of-concept trials
and will to assure a seamless transition into late-stage
development (Phase II-III trials)
Ability to lead and develop a group of CTPs to ensure scientific
and technical excellence of clinical development programs and
deliverables
Minimum 3 years' experience as a medical monitor with proven track
record designing and overseeing clinical trials, ideally both early
and late stage
Experience supervising CRO-driven studies
Experience with health authorities and regulatory submissions
Understanding of the clinical development process, and the role of
non-R&D functions: commercial, health outcomes, access,
medical
Proven ability to partner effectively with key internal and
external stakeholders
Excellent communication skills for conveying scientific data and
for internal and external interactions
Additional Qualifications/Responsibilities
Degree Requirements
MD preferably with appropriate sub-specialty training as
appropriate
At least 11years of relevant experience
Travel Required
Domestic and International travel may be required.
The starting compensation for this job is a range from
$308,000-354,000, plus incentive cash and stock opportunities
(based on eligibility). The starting pay rate takes into account
characteristics of the job, such as required skills and where the
job is performed. Final, individual compensation will be decided
based on demonstrated experience.
Keywords: National Guard Employment Network, Cambridge , CLINICAL DEVELOPMENT LEAD - CAMBRIDGE - MA, Healthcare , Cambridge, Massachusetts
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