Project Manager
Company: Alliance Foundation Trials, LLC
Location: Boston
Posted on: November 6, 2024
Job Description:
The Alliance for Clinical Trials in Oncology Foundation
(Foundation) is a foundation created to enhance and expand the
ability of the Alliance for Clinical Trials in Oncology (Alliance)
to conduct cancer clinical research and address important treatment
questions through large-scale clinical trials. Through efforts of
the Foundation in support of the Alliance, clinical trials and
laboratory research are conducted to discover new or improved ways
to prevent, treat, and cure many types of cancer, including
leukemia and lymphoma, and cancers of the breast, prostate, lung,
and gastrointestinal (GI) tract, and help educate the medical
community on methods of cancer diagnosis, treatment, and
prevention.In May 2014, the Foundation created the Alliance
Foundation Trials, LLC (AFT), respectively, a wholly-owned
subsidiary of the Foundation. AFT was also created to conduct
cancer clinical research and address medical care and treatment
through large-scale clinical trials involving various
industry-related partners.The Alliance Foundation Trials (AFT) is
looking for a Project Manager who manages the development,
implementation, and oversight of assigned AFT studies. This role
will also interact with pharmaceutical industry partners, vendors,
investigative sites and physicians to help AFT studies from
activation to closure. - Come join an organization full of
passionate, team-oriented professionals driven to change the face
of cancer. Benefits of working at the Alliance for Clinical Trials
in Oncology Foundation:
- 8 weeks of paid time off (including PTO, sick, and holidays)
during year one
- Medical, Dental & Vision plans with a 100% employer-paid option
for employees
- Tuition reimbursement stipends
- Continuing Education
- 3% employer match for retirement investments
- Annual Employee Performance Bonus Program
- Annual Cost of Living Adjustment
- 50% commuter reimbursement
- Healthy Work/Life balance and flexibility ROLE &
RESPONSIBILITIES
- Acts as operations lead on one or more AFT studies
- Serves as primary point of contact between AFT and
pharmaceutical industry partners associated with assigned AFT
studies
- Assists with the design, planning, implementation, conduct, and
management of clinical studies from initiation through
completion
- Represents AFT Clinical Operations on the cross-functional
project team, and liaises with medical, statistical, regulatory,
quality, and financial personnel
- Manages one or more AFT junior operations staff
- Oversees participating study vendors, including vendor
agreements, statements of work, and vendor budgets
- Manages overall study budget, including approvals of all
subject visit payments and vendor invoices for assigned
studies
- Oversees and manages the development of study-related documents
together with the scientific team and protocol development team
including, but not limited to, study protocol, informed consent
forms, laboratory manuals, eTMF plans, etc.
- Assists in the design, configuration, development, and
oversight of study-level systems such as EDC, eTMF, and CTMS
- Organizes, schedules, and leads study teleconferences and
in-person meetings with investigative sites, physicians, vendors,
and consultants as needed
- Serves as the central escalation point for all study issues
originating with component groups such as data management, site
management, site monitoring, laboratory management, etc., and
tracks escalated issues through to resolution
- Reviews study-related materials including, but not limited to,
monitoring reports, key performance metric reports, clinical trial
agreements, etc. as needed
- Works with the AFT Regulatory Manager to support regulatory
filings as needed
- Initiates and maintains study protocol(s) and associated
amendment tracking
- Oversees site activities on assigned studies, including
feasibility, activation, accrual, maintenance, and closure
- Tracks study progress and manages clinical timelines, including
regulatory document collection, IRB approval, enrollment,
management of clinical supplies, etc.
- Helps build and maintain relationships with site investigators
and other site study staff
- Assists with the reporting of clinical data for regulatory or
medical scientific purposes, including study publications
- Participates in the development and implementation of SOPs and
Clinical Operations processes and systems
- Handles other duties as assigned. QUALIFICATIONS AND EDUCATION
- A minimum of a BA/BS degree is required
- 4-6 years of Pharmaceutical, Academic Research Organization, or
Clinical Research Organization research and project management
experience required
- Willingness and capability to handle multiple studies and
responsibilities with shifting priorities
- Demonstrated project management skills; meeting project
timelines and budgets
- Prior experience assisting in the design, planning, and
implementation of a study from initiation through completion
- Solid understanding of the drug development process including
GCP and FDA Code of Federal Regulations
- Excellent organizational, leadership, and problem-solving
skills
- Excellent written and verbal communication skills
- Ability to successfully work both within a team and
independently
- Experience working in EDC (RAVE preferred), eTMF, and CTMS
systems
- Proficiency in Microsoft Office applications
- Ability to travel several times a year.
- Must be authorized to work in the U.S. PREFERRED SKILLS
- Degree in a health or science major preferred.
- Experience working in oncology research preferred The above
statements are intended to describe the general nature and level of
the work being performed by people assigned to this job. They are
not an exhaustive list of all duties and responsibilities
associated with it.
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Keywords: Alliance Foundation Trials, LLC, Plymouth , Project Manager, Executive , Boston, Massachusetts
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