Job summary
Job post source
This job is directly from Parexel
Job overview
The Study Manager/Project Manager at Parexel leads operational study management for clinical research studies, ensuring effective execution and oversight of study activities to support research collaboration.
Responsibilities and impact
The role involves developing study startup and monitoring plans, conducting feasibility assessments, managing vendor and drug supply coordination, leading risk planning, supporting protocol training, overseeing study delivery, and ensuring compliance with SOPs and quality standards.
Experience and skills
Candidates should have clinical trial/study management experience, knowledge of Good Clinical Practices, and at least 1-2 years of relevant experience depending on education level, with skills in vendor management, risk mitigation, data interpretation, and strong communication.
Company information
Parexel is a global biopharmaceutical services company specializing in clinical research and drug development support.
Job location and travel
This is a remote position available in the US and Canada.
Unique job features
The role includes technical oversight of CROs, responsibility for inspection readiness, and involvement in harmonizing study management processes for high-quality clinical trial data.
Company overview
Parexel is a global biopharmaceutical services organization that provides comprehensive drug development and regulatory consulting services to the pharmaceutical, biotechnology, and medical device industries. They make money by offering clinical research, regulatory consulting, and market access services that help clients expedite the development and approval of new therapies. Founded in 1982, Parexel has a long history of innovation in clinical research and has been involved in the development of many significant medical treatments.
How to land this job
Tailor your resume to emphasize your operational study management experience, focusing on managing clinical trials of limited complexity or specific study segments like recruitment and vendor oversight, as detailed in the job description at Parexel.
Highlight your expertise in developing detailed study startup and monitoring plans, conducting feasibility assessments, and leading risk planning processes, showcasing your ability to manage study deliverables and inspection readiness.
Apply through multiple platforms including Parexel’s corporate careers page and LinkedIn to maximize your application visibility and chances of being noticed by recruiters.
Connect with current employees in Parexel’s Research Collaboration Center of Excellence on LinkedIn; initiate conversations by complimenting recent company initiatives or asking for insights on the study management approach at Parexel to break the ice.
Optimize your resume for ATS by incorporating key terms from the job description such as 'study startup,' 'CRO oversight,' 'feasibility assessments,' 'risk mitigation,' and 'clinical trial budget management' to ensure your resume passes automated screenings.
Use Jennie Johnson’s Power Apply feature to automate tailored applications across multiple channels, identify relevant LinkedIn contacts for networking, and optimize your resume for ATS, allowing you to focus your time on preparing for interviews and enhancing your skills.
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