Create the solutions that drive global projects to success
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.
Project Director for a variety of studies ranging from cardiovascular to pediatric. Managing and mentoring Project Leaders in the US and Argentina.
Promoted to Associate Director in Project Management at Parexel working on post-approval smoking cessation treatment.
Joined Parexel as a Senior Project Lead mentoring and managing 5 project managers working on a phase IV smoking cessation treatment.
Associate Director for a large CRO developing online training program for new Clinical Research Associates.
Contribute to meaningful advances that benefit patients in need
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.
Co-founder of a specialty pharmaceutical company focusing on developing orphan indication products.
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.
Intensive Care Clinical Nurse in Oncology ICU participating in clinical trial data collection for phase I, II, and III studies.
Nurse’s Aide in Intensive Care Oncology Unit.
Contribute to meaningful advances that benefit patients in need
Joined Parexel as a Human Resources Operations Partner.
Human Resources Business Partner at leading pharmaceutical company.
Manager of Diversity Resources.
Assistant Manager for work/life balance programs.
Associate Personnel Representative at leading consumer goods manufacturer.
Be part of a diverse team that drives healthcare innovation
Promoted to Director IT Project and Programme Office, leading engineering projects for Wearable and Sensor devices with a view to streamlining Clinical Trials patient engagement and approaches.
Promoted to Associate Director of IT Program and Project Management at Parexel.
Joined Parexel as a Project Manager in the IT Project Program Office.
Senior Project Manager at a video game developer.
Development Manager working on maternity ultrasound software.
Lead Developer on software team.
Own the challenges that make you grow
Promoted to Senior Medical Writer, focusing on the development and support of modules, templates, master documents, and general guidelines for clinical documents intended for regulatory submission.
Began a new role working remotely as a Medical Writer II, researching and coordinating the development of clinical documents intended for submission to the FDA or other regulatory authorities.
Director of Imaging Operations leading a team of 13 Project Managers and the imaging of over 130 clinical trials.
Senior Project Manager, overseeing standardization of program operations and deliverables while leading a team of Project and Imaging Research Managers.
Promoted to Project Manager for clinical oncology trials.
Joined Parexel as an Imaging Research Associate on clinical trials utilizing medical imaging.
Physical Therapy Rehabilitation Aide.
Forge the relationships that elevate customer experience
Senior Director of Business Development at Parexel.
Associate in the Proposal Development department at Parexel.
Founder and Marketing Director of an IT venture company developing web related systems.
Managed the Therapy Development Group at a leading health care products manufacturer.
Relocated to the United States to pursue an MBA in Marketing.
Own the challenges that lead to innovation and growth
Led the project that streamlined Parexel's clinical operating model; driving effectiveness, reducing handoffs and increasing employee, client and site satisfaction.
Promoted to VP Clinical Operations, and relocated to the US in 2017.
Supported the implementation of Parexel’s new clinical operational model.
Promoted to Senior Director of Clinical Operations for the Americas, consolidating both North and South American regions.
Joined Parexel as Director of Global Monitoring Operations for Latin America.
Voice the ideas that get treatments to patients faster
Promoted to Senior Director of Clinical Application Development and Technology.
Promoted to Associate Director of IT.
Promoted to Senior Programmer.
Joined Parexel in Clinical IT.
Received Master's in Computer Applications.
Own the challenges, program your future
Advanced to Statistical Programming Manager, responsible for a dynamic, multinational team of over 12 people.
Increased responsibility, leading projects and managing small teams as a Principal Statistical Programmer / Associate Manager.
Promoted to Senior Statistical Programmer, participating in high profile trials for diverse range of sponsors, as main programmer.
Referred by a friend to join Parexel as a Statistical Programmer, taking the opportunity to further develop my programming skills in 4GL language using SAS® .
Functional Analyst for a financial provider working data sources and using SAS® tools
Junior Analyst for a consulting company, exploring and analyzing data to drive development.
Ruben – Associate Director in Project Management
Leslie - Vice President of Integrated Product Development
Deborah – Human Resources Operations Partner
Martin – Associate Director of IT Program and Project Management
Nicholas – Senior Medical Writer
Shigehiro – Business Development
Natalia – Clinical Operations
Naresh – Senior Director of Clinical Application Development and Technology
Pawel – Manager, Global Data Operations (GDO) Statistical Programming
By being hired into one of our Quality Management jobs at Parexel International, you’ll be a key member of the Parexel International team. Professionals in Quality careers come from a variety of backgrounds, bringing an assortment of knowledge and skills to every area of our business. A job in Quality at Parexel International may be waiting for you!
-Verify compliance with GxP guidelines/regulations, Parexel procedures and requirements, and sponsor requirements. -Actively participate in key internal project team meetings and facilitate quality discussions during these meetings. -Schedule and lead the project related Quality Forums. -Attend client meetings with project leadership to collaborate with and participate in discussions related to quality. -Provide support with investigation of Quality Issues (QIs) and support of QI management including classification of issues, assist in determination of root cause and consultation on appropriateness of corrective and preventive actions. -Provide audit and inspection support for assigned projects, including, where feasible, advising the project team during preparation and conduct of audits and inspections as per applicable SOPs. -Review and provide feedback on project related audit/inspection responses generated by project team members per applicable SOPs. -Represent Quality Management in audits and inspections as required. -Evaluate applicable project quality metrics. -Identify and evaluate potential risks and quality issues. -Collaborate with other PQRLs assigned to the client to identify quality trends. -Act as primary point of contact for communications with client quality representatives, and share lessons learned. -Report process gaps and participate in implementation of process improvement when required. -Participate in working groups as assigned to develop SOP and/or quality related processes. -Maintain compliance with training curriculum. -Consult process SMEs as necessary for guidance. -Support audits and inspections as host/co-host and provide support where needed. -Ability to work independently, take initiative, and have a flexible approach with respect to work assignments and new learning. -Multi-task with enthusiasm and prioritize workload with good organizational skills. -Ability to work effectively in a matrix environment and to demonstrate and foster teamwork.
-Exceptional interpersonal, verbal and written communication skills. -Client focused and detail oriented. -IT literate: experienced with Microsoft based applications and general knowledge of personal computer functions. -Relevant experience (e.g., in the pharmaceutical or CRO industry). -English proficiency (written and oral English). -Educated to degree level (technology, biological science, pharmacy or other health related discipline preferred) or equivalent qualification. -Clinical research experience.
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.