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  • 3322 West End Avenue
    Nashville, TN 37203

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Project Manager - Work From Home

Sarah Cannon Research Institute Clinical Operations • Nashville, TN

Posted 11 days ago

Job Snapshot

Degree - 4 Year Degree
Healthcare - Health Services
Management, Strategy - Planning


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Job Description

ClinicalProject Manager – Work From Home
SarahCannon Development Innovations isa full-service contract research organization (CRO) that is uniquelyfocused in oncology. Sarah Cannon Innovations offers strong scientificleadership, access to patients through Sarah Cannon Research Institute’s SiteManagement Organization (SMO) and relationships with other clinical sites, andexperience in drug development and delivery of clinical trials fromFirst-In-Man through registration level studies, making us the partner ofchoice for oncology.
Our differentiator is strong operational deliveryin partnership with our Site Management Organization and physician leaders todeliver your program efficiently.
Sarah Cannon Development Innovations works withSarah Cannon Research Institute strategic and network sites throughout theUnited States, along with investigators at sites outside of the Sarah CannonResearch Institute network. This reach allows Sarah Cannon DevelopmentInnovations to offer sponsors access to a diverse and varied patientpopulation, spanning multiple tumor types and disease stages. Theserelationships further enhance the depth and breadth of Sarah Cannon DevelopmentInnovations’ therapeutic expertise, enabling it to provide focused, strategicoperational support. This support ensures that clinical trials are conducted ina timely manner and reported with high-quality, registration-standard data.
Sarah Cannon, the global cancer enterpriseof Hospital Corporation of America (HCA), offers integrated cancer serviceswith convenient access to cutting-edge therapies for those facing cancer incommunities across the United States and United Kingdom.
**This is a Work From Homeposition and you can be located anywhere in the United States to be eligiblefor this role.
Summaryof Position:
Responsible for management of multipleassigned projects throughout all lifecycle phases. Ensures that all projectwork is completed to the client expectations, ensuring quality deliverables ontime and within budget and in accordance with SOPs, ICH GCP, applicableregulations, policies and practices. Serves as the principal liaison withclients to ensure effective and timely communication of project progress,issues, and plans for resolution of those issues. Provides leadership in thedevelopment of clinical trials and related documents. Works closely andeffectively with cross-functional teams. Provides input in business developmentproposals and attends bid defenses.
Duties and Responsibilities
Duties include but are not limited to:
  • Plan, track and manage all activity throughoutthe project lifecycle, including deliverables from all functional areas andvendors in accordance with the project scope
  • Develop project plans, timelines and statusreports and communicates with all applicable team members in and outside theorganization
  • Promote effective teamwork amongcross-functional teams and provide day to day direction for core team
  • Meet with team members on a regular basisregarding project tasks to ensure project milestones are met
  • Collect information and provide input to linemanagers on team performance against contract, customer expectations andproject baselines
  • Serve as primary project contact with clients toensure communication is maintained and reporting schedules are adhered to
  • Manage project budget, communicate deviationsfrom budget projections and propose solutions for budget deviations
  • Lead problem solving and resolution efforts.Provide proactive and creative recommendations on how to meet goals and handleidentified risks and deviations
  • Communicate and escalate unresolved issues atthe appropriate time and to the appropriate level of management
  • Ensure that work is conducted in compliance withprofessional standards and SOPs, and meet quality and timeline metrics
  • Build and maintain strong pharmaceuticalindustry sponsor and organizational team relationships for the success ofclinical trial management
  • Partner with other project managers to initiateimprovements to enhance the efficiency and the quality of the work performed onassigned projects
  • May participate in proposal development
  • May participate in the bid-defense process withguidance and supervision 
Knowledge:A body of information needed to perform a tasks; May be obtained througheducation, training or experience
  • Knowledge of FDA guidelines and GCP is required
  • Knowledge of budgeting and forecasting
Skills:The proficiency to perform a certain task
  • Professional writing and communication skills
  • Good teamwork skills
  • Organizational and prioritizing capabilities
  • Computer skills with ability using clinical trial databases, electronic data capture, MS Access or Excel
Abilities:An underlying, enduring trait useful for performing duties
  • Able to work with minimal direction
  • Resourceful with heightened analytical abilities and problem solving skills in a fast paced environment
  • Interpersonal skills, detailed-oriented and meticulous
  • Good judgment

Job Requirements

Minimum Qualifications
Minimum Required: Bachelor’s Degree (4 year program)
Preferred: Bachelor’s Degree (4 year program)
  • Clinical trial experience within pharmaceutical,biotechnology, CRO company and/or healthcare setting, i.e. managing thelogistics of clinical trial conduct, budgeting/forecasting, anddeveloping/executing project plans
  • Experience in healthcare research or otherscience related field
  • Previous experience as a Clinical ProjectManager for a CRO/pharma/biotech company
  • Demonstratedleadership skills
  • Experience in oncology clinical research phases I-III
  • Clinical trial experience within pharmaceutical, biotechnology, CROcompany and/or healthcare setting, i.e. managing the logistics of clinicaltrial conduct, budgeting/forecasting, and developing/executing project plans
  • Previous experience as a Clinical Project Manager
  • Experience in oncology clinical research phases I-III
  • Experience writing clinical protocols and other technical documents
  • Prior experience mentoring and/or training less senior team members
  • Experience managing study timelines, deliverables, and/or vendors
**Ifinterested in advancing your career with a growing leader in cancer researchplease apply today!

Job ID: 25319-4407
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Clinical Manager (Management)

Nashville, TN