43 results for cultures
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Global Head, Inside Sales
United States, Remote Sales -
Clinical Trial Manager -FSP
Singapore, Remote Clinical Trials, Functional Service Provider -
Senior Medical Writer - Structured Content Authoring - FSP
United States, Remote Canada, Alberta, Remote; Canada, British Columbia, Remote; Canada, Manitoba, Remote; Canada, New Brunswick, Remote; Canada, Newfoundland and Labrador, Remote; Canada, Northwest Territories, Remote; Canada, Nova Scotia, Remote; Canada, Nunavut, Remote; Canada, Ontario, Remote; Canada, Prince Edward Island, Remote; Canada, Quebec, Remote; Canada, Saskatchewan, Remote; Canada, Yukon, Remote Medical Writing, Functional Service Provider -
Senior / Principal Regulatory Compliance Consultant - QC Microbiology
United States, Remote Regulatory Affairs -
Clinical Research Manager- FSP
Canada, Quebec, Remote Clinical Trials, Functional Service Provider -
Clinical Research Associate II
Taiwan, Taipei Clinical Trials, Clinical Research Associate -
Clinical Research Associate I
Taiwan, Taipei Clinical Trials, Clinical Research Associate -
Clinical Research Associate I/II/Senior-FSP
Taiwan, Taipei Clinical Trials, Clinical Research Associate, Functional Service Provider -
Clinical Research Associate I - II
Australia, North Ryde Australia, Remote Clinical Trials, Clinical Research Associate -
Clinical Research Associate (Japanese/Korean Speaker) - FSP
South Korea, Remote Clinical Trials, Clinical Research Associate, Functional Service Provider -
Clinical Research Associate - FSP
Argentina, Remote Clinical Trials, Clinical Research Associate, Functional Service Provider -
Initiation Clinical Research Associate I
Hong Kong Clinical Trials -
Initiation Clinical Research Associate I
Hong Kong Clinical Trials -
iCRA II
India, Bengaluru Clinical Trials, Clinical Research Associate -
Clinical Research Associate I/II/Senior
Taiwan, Taipei Clinical Trials, Clinical Research Associate
21 Content Pages Found
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Meet Zulma, Senior Regulatory Affairs Manager
Discover Zulma's inspiring career in regulatory affairs at Parexel. From mentoring talent to dancing across cultures, learn how she balances technical expertise with empathy in clinical research, always keeping patients at the heart of her work. -
Meet Diana, Associate Director, Supply & Logistics Portfolio Management
Diana shares her journey at Parexel, from starting as a Project Specialist in Argentina to leading a team of 10 logistics experts in Berlin as an Associate Director. She discusses the work of her Supply & Logistics team, the strong team culture, and how they connect their work to Parexel's Patients First core value. -
Meet Lukasz, Clinical Research Associate II
Follow Lukasz's journey from creating stained glass to frontline clinical research. His candid perspective reveals the contrasting rhythms of office and site days, the human connections behind the data, and how Parexel's supportive environment enables both professional excellence and personal passions like travel and a -
Meet Iris, Data Manager II at Parexel
Read more about Iris, Data Manager II, who values patient impact, balances technical expertise with compassion, and champions quality data. -
Initiation CRA Qualifications, Skills and Experience
Discover the qualifications, education, experience, and skills needed to be a successful Initiation Clinical Research Associate (iCRA) -
Meet Sherry, Clinical Research Associate I
Explore life as a CRA I at Parexel. Learn how passion for patient care and continuous learning drive innovative healthcare solutions. Join Sherry's CRA I journey in advancing clinical trials. -
Meet Yoela, a Site Feasibility Liaison
Yoela Murillo is a Site Feasibility Liaison, but if you happen to catch her outside the office, you might see her singing in her community choir, dancing to her favorite music, tending to her plants or absorbed in watching a soccer match. Yoela has worked for Parexel for over three years, and she discusses what makes her proud of her work and how she always keeps "Patients First". -
Meet Vivian, a Site Intelligence Director
Discover how Vivian’s leadership in Site Intelligence is transforming feasibility, operations, and data use at Parexel. -
What does a Regulatory Affairs Consultant do?
Explore the Regulatory Affairs Consultant role at Parexel: key responsibilities, tools, collaboration, career growth, and work flexibility in clinical research. -
Meet Stella, a Clinical Feasibility Associate Director
Explore Stella’s 18-year journey at Parexel, which she describes as the best place to grow, learn and become a Clinical Feasibility Associate Director. -
Meet Brian, a Data Management Manager
Meet Brian, a Data Management Manager at Parexel who transformed from clinical researcher to Data Manager. Discover how Parexel nurtures talent in Clinical Data Analytics, offering exciting career paths and innovative opportunities. Learn valuable insights for aspiring CDAs and see why Parexel is at the forefront of healthcare data management. -
Regulatory Affairs Opportunities
Help shape the future of drug development, streamline approval processes, and safeguard patient well-being. Advance your career and explore Parexel's diverse roles in Regulatory Strategy, Regulatory Affairs, Compliance, Consulting, and more. -
Meet Chrishni, a Senior Project Leader with an exciting global journey
Discover Chrishni's inspiring journey at Parexel, where her love for France led her to relocate from Australia and thrive in her career based in Lyon. She enjoys collaborating with her team and finding a harmonious work-life balance to indulge in her passions. -
Location: Argentina
Work where you will find flexible working options, a supportive atmosphere, constant learning, and more. -
Meet Angeli: Senior Project Specialist
Angeli shares what it is like to work as a Project Specialist and with her colleagues within the Project Planning & Support department.
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