Own the challenges that lead to innovation and growth
Promoted to Head of Biotech Operations for Americas East, helping clients develop novel therapies with a focus on patient needs.
Advanced to Corporate VP Clinical Operations to lead Site Monitoring for Americas, Europe and SE Asia.
Streamlined Parexel’s clinical operations model; driving effectiveness, and increasing employee, client and site satisfaction.
Promoted to VP Clinical Operations, and relocated to the US in 2017.
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.
Create the solutions that drive global projects to success
Promoted to Senior Director, Project Management. Taking on management responsibilities for dedicated Enterprise accounts and enhancing his contributions to Parexel’s Global Project Leadership.
Managing Project Director role for dual Enterprise accounts, with a focus on client delivery and satisfaction in order to bring in new awards and expand growth.
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.
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.
Be part of a diverse team that drives healthcare innovation
Advanced into Senior Manager, Human Resources
Promoted to Manager, Human Resources Operations
Joined Parexel as a Human Resources Operations Partner.
Human Resources Business Partner at leading pharmaceutical company.
Manager of Diversity Resources.
Contribute to meaningful advances that benefit patients in need
Joined the Scientific Data Organization as Scientific Data Technology Director, creating agile access to real world data, bringing best in class technology solutions to Parexel services, and harnessing data to transform therapy development for patients.
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.
Own the challenges that make you grow
Promoted to Senior Medical Writer, focusing on the development and support of 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.
Forge the relationships that elevate customer experience
Corporate Vice President, General Manager – Japan
Vice President, Growth Accounts
Senior Director of Business Development at Parexel.
Associate in the Proposal Development department at Parexel.
One of the founders and Marketing Director of an IT venture company developing web related systems
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
Promoted to Senior Manager, Statistical Programming, with increasing responsibilities for department development and team supervision.
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® .
Natalia – Head of Biotech Operations for Americas East
Ruben – Senior DirectorProject Management
Deborah – Senior Manager Human Resources
Martin Scientific Data Technology Director
Nicholas – Senior Medical Writer
Shigehiro – Corporate Vice President, General Manager – Japan
Naresh – Senior Director of Clinical Application Development and Technology
Pawel – Senior Manager Statistical Programming
Jobs at Parexel
Are you ready to make your mark in the healthcare industry by taking your work seriously, demonstrating empathy, and acting with heart? When our values align, there's no limit to what we can achieve. We work with the top 50 global pharmaceutical companies, the top global biotech companies, and hundreds of small and emerging companies. We've supported the development of some of the most important treatments of our time, including nearly all of the 50 top-selling drugs currently on the market. Join us and you'll make a profound difference in millions of lives. We're not just the people with expertise, we're the people with heart.
Parexel is seeking Nurses with at least 1 year of experience to work in our Early Phase Clinical Unit in Baltimore, MD. We currently have daytime fulltime and part time positions available. The shifts are 6,8, or 12-hours long and include weekend rotations and an occasional night shift.
Execute and coordinate a variety of specialized clinical research activities ensuring that established protocols are implemented and followed.
Monitor patient and participant status and safety. (This role is less physical than other nursing positions as the working environment involves mostly healthy people.)
Collect and organize research data.
Educate patients and family members, for patient studies, and healthy participants about treatments and possible side effects and complications.
Support Standard Operating Procedures (SOPs), Good Clinical Practices, and all work processes to ensure the efficient and compliant clinical operation of the Early Phase Clinical Unit (EPCU).
Assume responsibility for patient care and study conduct assignments.
Ensure all study laboratory and medical tests are completed, and that eligibility requirements specific to the assigned study are met.
Assess compliance, symptoms, etc. per study protocol.
Arrange for pre/post procedure laboratory work to be performed.
Ensure that all established timelines relating to areas of responsibility and assigned projects are met.
Contribute to the development and implementation of study/research objectives.
Demonstrate Guest and Staff Relations standards in all activities.
Assess, monitor, record, and report patient’s condition and reaction to drugs and treatments to the appropriate physician.
Dispense medication as directed.
Collect and prepare data.
Organize and enter data into case report forms.
Enter data into databases when required.
Assist physicians in completing flow sheets in medical records and progress notes.
Update and maintain the contents of the Clinical Study File.
Perform or arrange for phlebotomy, urine collection, sample preparation, storage and shipment of samples, drug dispensing, and follow GCP quality study documentation.
Act as participant advocate in the conduct of clinical studies.
Perform equipment and drug checks as required by departmental policy.
Report equipment failures to the Clinical Services Leader.
Arrange for replacement of expired or used supplies in conjunction with the Clinical Services Leader.
Support the implementation and application of ClinBase™ in the EPCU.
Participate in quality improvement initiatives.
Assist project coordinators and project managers in reviewing informed consent documents, source documents, and case report forms.
Review consent forms, treatment schemas, and side effects of drugs with study participants and research team members.
Administer Informed Consents according to Good Clinical Practice guidelines.
Discuss potential adverse events and study schedules with study participants.
Assign tasks and clinical procedures to appropriately trained research assistants and research technicians.
Responsible for clinical trial material accountability in coordination with EPCU Pharmacy Technician and Pharmacist.
Maintain security of blinded code and notifies physician of participant conditions, which may require blinded code identification.
Assume other duties and responsibilities as assigned.
The above responsibilities are a general description of the level and nature of the work assigned to this classification and is not to be considered as all-inclusive.
Excellent organizational and communication skills. Must be able to communicate well with people and Doctors.
Attention to detail.
Self-directed and work with minimal supervision.
Invasive pressure monitoring, emergency care and comprehensive assessment skills are also highly desirable.
Computer skills and familiarity with research process.
Physical Requirements: Moving and lifting patient, pushing stretchers, moving heavy monitors, visual and auditory acuity, manual dexterity, exposure to body fluids.
BSN or relevant work experience such as MedSurg, ICU, Step-down nurses, school nurses and stay-at-home nurse experience preferred.
Licensed RN, BLS certification.
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.