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Project Manager Resume Example

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PROJECT MANAGER
Professional Summary
Highly motivated and result driven professional seeking a rewarding career in management. Project manager with a three year record of successful launching, directing and managing of medium scale projects by performing management functions such as: planning, scheduling, organizing, and tracking processes, ensuring the feasibility of each project. Keen understanding of business priorities, genuine team player committed to managing operations and projects flawlessly while contributing to revenue- producing activities. Cross-functional communicator easily interfaces with high-profile staff, vendors, and customers. Versatile, innovative, and loyal management professional able to see the "big picture" while staying on top of all the details. Strong leader well versed in developing strategic road maps in collaboration with senior leaderships to develop, plan and implement innovative solutions to far exceed level of research development and project management.
Core Qualifications
  • Training and development
  • Financial records and processing
  • Reports generation and analysis
  • Work flow planning
  • Project development and lifecycle
  • Operations management
  • Budgeting and forecasting
  • Process improvement
  • Risk management
  • Cost reduction and containment
  • Contract management
Experience
Project Manager
February 2013 to CurrentCompany Name － City, State
  • Provide technical, contractual and operational support for the National Cancer Institute Biospecimen and Biorepository Research and Cancer Research Branch.
  • Coordinate technical and operational activities within the planned time frame / budget.
  • Perform qualification visits and monthly site and audit visit in accordance to management plan.
  • Develop and initiate internal processes to improve project delivery within specific timeframes.
  • Responsible for resources required for completion of a project and allocated resources accordingly.
  • Define the resources required for completion of a project and allocated resources accordingly.
  • Collaborate with team members and sub-contractors to address action items, risks, and issues.
  • Monitor external environment with respect to new technology, methodology, regulations and guidelines emerging to support/guide or govern the conduct of procurements research projects.
  • Collaborate with management teams to deliver assigned programs - Develop group and individual timelines, assess/identify potential bottlenecks in each project/program process.
  • Perform extensive technical reviews for prospective projects, gathering details utilized for pricing project services, and providing supportive documentation for RFP replies to sponsors; Acting Contracting Official Representative.
Clinical Project Coordinator
August 2012 to February 2013Company Name － City, State
  • Planned, managed and coordinated all special project activities to ensure goals and objectives of such projects are accomplished within the specified time frame and funding parameters.
  • Performed and managed on-site duties and responsibilities with the site PI.
  • Assumed major responsibility in handling time line management of other functional areas, including data management, regulatory affairs, safety, and clinical quality assurance.
  • Managed concurrent out-patient pharmaceutical research studies for cancer clinical trials.
  • Coordinated research subject's clinical treatment and follow-up care and help facilitate their participation in accordance with regulations and as required by the study protocol.
  • Project leader for the collection and management of clinical study data.
  • Supervised 5 staff members who performed data entry, and provided recommendations concerning time saving methods in data collection.
  • Performed data validity and accuracy in compliance with quality control requirements.
  • Assisted Principle Investigator in development and management of budget and financial reporting.
Clinical Study Coordinator
September 2011 to August 2012Company Name － City, State
  • Participated in protocol clinical development and planning for assigned studies.
  • Executed and coordinated a variety of specialized research activities ensuring that established protocols are implemented and followed.
  • Supervised 10 study team members.
  • Provided clinical monitoring for assigned studies.
  • Collected and organized research data and assist in preparation of regulatory documents (IRB submission and FDA audits).
  • Collaborated with the PI and internal department to prepare a categorized budget and justification.
  • Scheduled project specific training and unit in-services to train clinical staff on protocols, GCP, ICH, GLP, GMP guidelines.
  • Responsible for feasibility studies, screening, recruiting, consenting, and retention of patients.
  • Developed and distributed scientific study materials for presentations presented to investigator sites, sponsors and team members.
  • Assisted in developing and revising reports and organizing information and presenting findings involving medical and scientific subjects.
  • Participating in monitor visit, SIV's, and study close out.
Research Technician
February 2010 to September 2011Company Name － City, State
  • Assigned to clinical research trial for the development of new drugs for treating multiple clinical areas.
  • Serve as a hands-on technician performing on site clinical analysis.
  • Performed study-related tasks, as directed in accordance with protocol and project requirements.
  • Provided support to research projects by following protocol specifications, ICH and GCP guidelines, and SOPs.
  • Record and submit serious and non-serious adverse events for patient safety.
  • Assist coordinator and team to perform QC analysis on all clinical trial start-ups and daily work flow in accordance with protocol specifications.
Data Associate
June 2009 to October 2009Company Name － City, State
  • Reviewed and processed clinical trial data ensuring accuracy and consistency of all clinical databases.
  • Performed case report tracking, reviewed CRF/e-CRF, and validated clinical data.
  • Provide accurate and consistent clinical data to sponsors and other internal departments to support daily business needs.
  • Managed to write queries and updated the database accordingly.
Education
Bachelor of Science : Chemistry Biology, 5 2009Shenandoah University － City, StateChemistry Biology
Master of Science : Biotechnology Management, 12 2014University of Maryland, University College － City, StateBiotechnology Management
Professional Affiliations

Shenandoah University, Alumni Association


Skills

Project Management, Budget Management, Statistical Analysis, Data Management, Databases, Business feasibility, Financial Reporting, Clinical Research, Biorespository Research GCP, GLP, GMP, Organizing, Presenting, Pricing, Process Improvident, Project Requirements, Project leadership, Quality Management, Recruitment, Research Development, RFP.

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Resume Overview

School Attended

  • Shenandoah University
  • University of Maryland, University College

Job Titles Held:

  • Project Manager
  • Clinical Project Coordinator
  • Clinical Study Coordinator
  • Research Technician
  • Data Associate

Degrees

  • Bachelor of Science : Chemistry Biology , 5 2009
    Master of Science : Biotechnology Management , 12 2014

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