CONTRIBUTE TO MEANINGFUL ADVANCESTHAT BENEFIT PATIENTS IN NEED
2014
Vice President of Integrated Product Development, leading a team of global regulatory affairs experts to help clients develop products more quickly and reach patients in need.
2006
Co-founder of a specialty pharmaceutical company focusing on developing orphan indication products.
1998
Director at several biopharmaceutical companies. Coordinated large clinical studies that spanned 6 continents, 30 countries, and 200 sites related to phase III sepsis and inflammatory disease studies.
1988
Intensive Care Clinical Nurse in Oncology ICU participating in clinical trial data collection for phase I, II, and III studies.
1979
Nurse’s Aide in Intensive Care Oncology Unit.
CREATE THE SOLUTIONSTHAT DRIVE GLOBAL PROJECTS TO SUCCESS
2017
Assumed the role of Global Project Leadership Training Coordinator, ensuring new PLs are properly inducted in all regions, while leading cross regional meetings to review and update training materials for PLs.
2016
Project Director for a variety of studies ranging from cardiovascular to pediatric. Managing and mentoring Project Leaders in the US and Argentina.
2015
Promoted to Associate Director in Project Management at PAREXEL working on post-approval smoking cessation treatment.
2012
Joined PAREXEL as a Senior Project Lead mentoring and managing 5 project managers working on a phase IV smoking cessation treatment.
2003
Associate Director for a large CRO developing online training program for new Clinical Research Associates.
EMBRACE THE OPPORTUNITIESFOR PERSONAL AND PROFESSIONAL GROWTH
2015
Joined PAREXEL as a Human Resources Operations Partner.
2013
Human Resources Business Partner at leading pharmaceutical company.
1999
Manager of Diversity Resources.
1993
Assistant Manager for work/life balance programs.
1989
Associate Personnel Representative at leading consumer goods manufacturer.
BE PART OF A DIVERSE TEAMTHAT DRIVES HEALTHCARE INNOVATION
2017
Promoted to Director IT Project and Programme Office, where I am leading engineering projects for Wearable and Sensor Devices, with an view to streamlining Clinical Trials patient engagement and approaches.
2016
Promoted to Associate Director of IT Program and Project Management at PAREXEL.
2013
Joined PAREXEL as a Project Manager in the IT Project Program Office.
2005
Senior Project Manager at a video game developer.
1997
Development Manager working on maternity ultrasound software.
1994
Lead Developer on software team.
OWN THE CHALLENGESTHAT MAKE YOU GROW
2017
Began a new role working remotely. As Medical Writer II, Scientific and Medical Services, I research, create, edit, and coordinate the development of independent review charters (IRC), reviewer manuals, imaging case report forms (CRFs), and other clinical documents intended for submission to the FDA or other regulatory authorities.
2015
Director of Imaging Operations leading a team of 13 Project Managers and the imaging of over 130 clinical trials.
2007
Senior Project Manager, overseeing standardization of program operations and deliverables while leading a team of Project and Imaging Research Managers.
2004
Promoted to Project Manager for clinical oncology trials.
2003
Joined PAREXEL as an Imaging Research Associate on clinical trials utilizing medical imaging.
2001
Physical Therapy Rehabilitation Aide.
FORGE THE RELATIONSHIPSTHAT ELEVATE CUSTOMER EXPERIENCE
2016
Senior Director of Business Development at PAREXEL.
2003
Associate in the Proposal Development department at PAREXEL.
2000
Founder and Marketing Director of an IT venture company developing web related systems.
1999
Managed the Therapy Development Group at a leading health care products manufacturer.
1995
Relocated to the United States to pursue an MBA in Marketing.
OWN THE CHALLENGES THATLEAD TO INNOVATION AND GROWTH
2013
Promoted to Senior Director of Clinical Operations for the Americas, consolidating both North and South American regions.
2012
Joined PAREXEL as Director of Global Monitoring Operations for the Latin America region.
2008
Associate Director of Clinical Management leading the implementation of a study start-up model in Latin America for a major CRO.
Natalia's leap forward came after joining the world of Clinical Research, where she progressed to the level of Clinical Operations Manager. In addition, Natalia took on responsibility for Site Start Up, extending her reach beyond Argentina to the whole of Latin America.
2000
Biochemist for a hematology lab.
1997
Team member connecting at-risk populations with primary healthcare and nutrition.
Leslie - Vice President of Integrated Product Development
Ruben – Associate Director in Project Management
Deborah – Human Resources Operations Partner
Martin – Associate Director of IT Program and Project Management
Nicholas – Medical Writer II, Scientific and Medical Services
We currently have an exciting opportunity for an individual with a strong background in Early Phase (Phase I and II) Drug Development who can take on a senior role within the Early Project Development (EPD) group as a Solution Consultant, Early Phase. This position can be regionally home based in any location in US.
The Early Phase Solutions Consultant will be a recognized professional in her/his area (technical, functional or therapeutic), with experience in the design, operational conduct and successful delivery of Solutions globally. S/he works in partnership with Enterprise Accounts, Growth Accounts, Commercial Operations and SBUs to optimize new business awards through the development of compelling operational and technical strategies and business solutions to support current and future client needs. These strategies will include in-depth risk assessments and scenario plans.
Qualifications
Skills
Demonstrates an energetic, 'make it happen' attitude, capable of thriving in a complex matrix environment with an ability to build strong cross functional relationships.
Strong understanding of commercial ecosystem and awareness of industry trends in their area of expertise through active participation in leading industry forums and professional organizations as well as maintaining awareness of relevant changes in global regulations.
Ability to see the strategic view while employing pragmatic approaches to delivery
Excellent interpersonal, verbal and written communication skills with delivery to all business levels.
Independent thinking with a flexible attitude to work assignments and developing new capabilities.
Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail.
Demonstrated ability to communicate complex ideas in a simple, understandable and compelling manner
Exceptional analytical and problem-solving skills
Knowledge, Experience & Education
Multiple years of experience in Pharma and CRO industries
15+ year of experience in strategic drug development planning or significant involvement in planning clinical, technical or operational strategies
Extensive experience in Early Phase Drug Development and developing strategy
Therapeutic experience in any of the following required; Oncology, Cardiovascular, Respiratory, Generics, Vaccines, and Metabolic
PAREXEL is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
It has been brought to our attention that there has been fraudulent activity by scammers attempting to represent themselves as PAREXEL employees or recruiters. These individuals are attempting to reach potential job seekers through online chat interviews and sending false offer letters, representing PAREXEL without our consent. If you’re concerned that you’ve been contacted by an unauthorized PAREXEL recruiter or employee, please notify Jobs@PAREXEL.com. You may also report suspicious fraudulent activity to your local law enforcement agency or the FBI. Thank you.
