Senior Project Manager
Company: Precision Medicine Group
Location: Carlsbad
Posted on: April 20, 2025
Job Description:
Senior Project Manager
at Precision Medicine Group (View all jobs)
Remote, United States
The Senior Project Manager plans, directs, coordinates, and
delivers activities for designated clinical study projects to
ensure that project objectives of quality, scope, cost, and time
are accomplished.
Essential functions of the job include but are not limited
to:
- Serve as primary point-of-contact and primary escalation point
to the client
- Coordinate and oversees all functional services including
external vendors to the established timeline and budget
- Manage the study budget, ensuring project remains within scope
and that any out of scope activities are identified early and
handled as appropriate. Independently drive the CO to completion
and execution with support as needed.
- Maintain integrated collaboration with clinical operations in
the delivery and participates in clinical activities as
appropriate. For projects of very limited scope (i.e. number of
sites), Sr. PM may assume all clinical activities
- Manage the financial health of assigned studies, including
oversight of the project profitability, billable project hours, and
compliance with on time, accurate billing and forecasting to
support business objectives.
- Develop robust and comprehensive project plans, including
timelines and proactive risk management and mitigation, to guide
all parameters of trial execution with consistency and quality
- Ensure Quality management for assigned projects, including eTMF
Inspection readiness, implementation of quality notification
incident forms and / or corrective and preventative action plans to
address any quality findings.
- Maintain integrated collaboration with all functional
operations in the delivery of the program and review as necessary
of other study documentation
- Establish tracking metrics to monitor trial and team progress
towards project goals
- Prepare project status updates and report on progress to
clients and senior management, including reporting on key
performance indicators, offering solutions and opportunities as
they arise
- Leads both internal and client meetings and set expectations
for the project team
- Communicate effectively with client and Precision management to
relay protocol/study issues including any deviations and implements
necessary actions in response to those issues
- Ability to conduct formal presentations to a wide variety of
audiences including colleagues, investigative staff, and clients
including Bid Defences with proficiency
- Ensure study specific training is implemented in collaboration
with functional areas and ensure study specific training compliance
for the duration of the project
- Support business development and marketing activities as
appropriate, including travel to Bid Defense meetings as
required
- Perform other duties as assigned by management
- Remain compliant with organisational training, time-reporting
and any other administrative duties as required
- Provides on-going feedback, for functional team members
including annual performance reviews
Qualifications:
Minimum Required:
- North America: Bachelor's degree or equivalent combination of
education/experience in science or health-related field. Advanced
degree preferred
- EU: Degree or equivalent combination of education/experience in
science or health-related field. Advanced degree preferred
- Minimum of 7 years of clinical research experience or proven
competencies for this position and a minimum of 4 years of direct
project management experience
- Experience in managing complex and global trials
- Ability to travel domestically and internationally including
overnight stays
Other Required:
- Experience with Microsoft Office Products (Outlook, Word,
Excel, PowerPoint) Microsoft Project, eTMF, EDC and CTMS
- Proven communication and interpersonal skills to effectively
interface with others in a team setting
- Proven organizational skills, attention to detail, and a
customer service demeanour
Competencies:
- Demonstrates knowledge of ICH-GCP, relevant Precision SOPs, as
well as the ability to implement such items
- Proven knowledge of project management techniques and
tools
- Direct work experience in a global, cross-functional project
management environment
- Good understanding of cross-functional management
- Good understanding of project planning, risk management and
change management with an awareness of appropriate escalation
- Proven experience in strategic planning, risk management and
change management
- High level of integrity and must inspire and demand the highest
standards from a professional and ethical perspective
- Ability to lead and inspire excellence within a study team
- Ability to create an environment where study team members have
a sense of ownership that will lead to increases in productivity
and efficiency
- Results oriented, accountable, motivated and flexible
- Proven time management, negotiation, critical thinking,
decision making, analytical and interpersonal skills
- Proven presentation, verbal and written communications
skills
- Good understanding of project management software
- In depth proven experience in pharmaceutical and/or device
research required
- Preferred: experience with oncology & cell and/or gene
therapy
Precision is required by law in some states or cities to include a
reasonable estimate of the compensation range for this role. This
compensation range takes into account the wide range of factors
that are considered in making compensation decisions including but
not limited to: skill sets, experience and training, licensure and
certifications, and other business and organizational needs. The
disclosed range estimate has not been adjusted for the applicable
geographic differential associated with the location at which the
position may be filled. At Precision, it is not typical for an
individual to be hired at or near the top of the range for their
role and compensation decisions are dependent on the facts and
circumstances of each case. This role is also eligible for a
discretionary annual bonus, health insurance, retirement savings
benefits, life insurance and disability benefits, parental leave,
and paid time off for sick leave and vacation, among other
benefits.
Reasonable estimate of the current range
$113,900 - $170,900 USD
Any data provided as a part of this application will be stored in
accordance with our Privacy Policy. For CA applicants, please also
refer to our CA Privacy Notice .
Precision Medicine Group is an Equal Opportunity Employer.
Employment decisions are made without regard to race, color, age,
religion, sex, sexual orientation, gender identity, national
origin, disability, veteran status or other characteristics
protected by law.
If you are an individual with a disability and require a reasonable
accommodation to complete any part of the application process or
are limited in the ability or unable to access or use this online
application process and need an alternative method for applying,
you may contact Precision Medicine Group at
QuestionForHR@precisionmedicinegrp.com .
It has come to our attention that some individuals or organizations
are reaching out to job seekers and posing as potential employers
presenting enticing employment offers. We want to emphasize that
these offers are not associated with our company and may be
fraudulent in nature. Please note that our organization will not
extend a job offer without prior communication with our recruiting
team, hiring managers and a formal interview process.
Keywords: Precision Medicine Group, Mission Viejo , Senior Project Manager, Executive , Carlsbad, California
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