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Clinical Research Nurse
PAREXEL International Corporation
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 FSP, 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 Director
Deborah – Senior Manager
Scientific Data Technology Director
Nicholas – Senior Medical Writer
Shigehiro – Corporate Vice President, General Manager – Japan
Naresh – Senior Director of Clinical Application Development
Pawel – Senior Manager
Jobs at Parexel
Are you ready to make your mark in the healthcare industry by taking your work seriously, demonstrating empathy, and acting
? 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
Clinical Research Nurse
For the Daytime Fulltime or Part-time positions, the hours are:
Primarily weekdays with weekend work rotation. 6, 8, and 12-hour dayshifts available.
Occasional nightshift required.
Self-scheduling and flexibility according to unit needs.
Nursing experience needed:
At least 1 year nursing experience.
Mostly healthy adults and on occasion a child.
On occasion an adult with a specific diagnosis.
This is a 24/7 in-house unit where participants stay for various lengths of time as determined by different studies. Participants are housed in dormitory-style accommodations, with multiple participants assigned to one room. The nurses oversee the day-to-day administration and operations of the unit.
The overall goal is to introduce medication or instruments to be tested for future public use for a variety of indications or illnesses. The nurses are also primarily responsible for investigational product administration via multiple routes, including, but not limited to, IV, IM, SC, PO, Topical, Inhalation etc. The nurses are attentive to the safety of participants and possible side-effects.
Nurses work closely with an interdisciplinary team, which includes Clinical Research Coordinators, Project Managers, Medical Team, and Research Assistants, in order to plan for and manage clinical trials.
Support Standard Operating Procedures (SOPs), Good Clinical Practices (GCP), and all work processes to ensure the efficient and compliant clinical operation of the Early Phase Clinical Unit (EPCU).
Assumes responsibility for patient care and study conduct assignments. Ensures that all study laboratory and medical tests are completed, and that eligibility requirements specific to the assigned study are met. Assesses compliance, symptoms, etc. per study protocol. Arranges for pre/post procedure laboratory work to be performed.
Ensures that all established timelines relating to areas of responsibility and assigned projects are met.
Participates and may direct identification and enrollment of study participants. Contributes to the development and implementation of study/research objectives.
Demonstrates Guest and Staff Relations standards in all activities.
Assesses, monitors, records, and reports patient’s condition and reaction to drugs and treatments to the appropriate physician. Dispenses medication as directed.
Collects and prepares data. Organize and enter data into case report forms. Enter data into databases when required. Assists physicians in completing flow sheets in medical records and progress notes. Updates and maintains the contents of the Clinical Study File.
Performs or arranges for phlebotomy, urine collection, sample preparation, storage and shipment of samples, drug dispensing, and follows GCP quality study documentation.
Acts as participant advocate in the conduct of clinical studies.
Excellent organizational and prioritizing skills required
Excellent communication skills required. The ability to communicate well with people and doctors are essential.
Attention to detail is critical.
Must be self-directed and often work with minimal supervision.
Emergency care and comprehensive assessment skills are also highly desirable.
Knowledge and Experience:
Desired at least 1-year nursing experience
Strong computer proficiency with Microsoft Office (Word, Excel, Outlook) is preferred.
Familiarity with the research processes are highly desirable.
Working Schedule: Because the clinic is a 24/7 in-house unit, schedule will include shift rotation and weekends as the workflow dictates. Day shift primarily include weekdays with weekend work rotation. 6, 8, and 12-hour dayshifts available. Occasional nightshift is required. Although self-scheduling applies, flexibility is necessary to accommodate unit needs and changes.
Physical Requirements: Moving and lifting patient, pushing stretchers, moving heavy monitors, visual and auditory acuity, manual dexterity, exposure to body fluids.
BSN preferred or relevant work experience.
Current Maryland Registered Nurse License.
Current Basic Life Support (BLS) certification.
ACLS certification required within 6 months of start date
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.
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