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Clinical Project Manager Jobs (On-site work)

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Clinical Project Manager
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Lead clinical studies from planning to regulatory submission as a Clinical Project Manager in Paris. This permanent role requires 6-8 years of Phase II/III experience in pharma/CRO, plus expertise in FDA/EMA dossiers. International development experience and fluency in English are essential. Onco...
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France , Paris
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Not provided
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AB SCIENCE
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Until further notice
Clinical Engineering Project Manager
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Join Sodexo's HTM team as a Clinical Engineering Project Manager in Omaha, NE. Oversee capital planning for medical devices, manage projects from start to finish, and analyze service contracts. Requires 3-5 years of clinical engineering and project management experience in healthcare. Enjoy compr...
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United States , Omaha
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50.00 USD / Hour
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Medasource
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Until further notice
Clinical Engineering Project Manager
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Seeking a Clinical Engineering Project Manager for a 3-4 month assignment in Cleveland, OH. You will oversee capital planning, medical device acquisition, and service contract analysis for large-scale HTM projects. The ideal candidate has a clinical engineering background and 3-5 years of healthc...
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United States , Cleveland, Ohio
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50.00 USD / Hour
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Medasource
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Until further notice
Explore rewarding Clinical Project Manager jobs and discover a pivotal career at the heart of medical innovation. A Clinical Project Manager (CPM) is a specialized professional who orchestrates the planning, execution, and delivery of clinical trials, ensuring they are conducted on time, within budget, and in full compliance with regulatory standards. These leaders serve as the central hub, integrating the efforts of cross-functional teams to advance new drugs, medical devices, or therapies from concept to market. Professionals in these roles are typically responsible for the end-to-end management of one or more clinical studies. Common responsibilities include developing detailed project plans, timelines, and budgets. They lead the creation and finalization of key documents like study protocols, amendments, and final clinical study reports. A core part of the job involves serving as the primary point of contact, managing relationships with internal stakeholders—such as clinical operations, data management, biostatistics, and medical writing teams—as well as external partners like Contract Research Organizations (CROs), investigative sites, and key opinion leaders. They proactively identify and mitigate risks, solve complex operational challenges, and ensure consistent communication across all parties. Furthermore, CPMs play a crucial role in regulatory compliance, often contributing to the preparation of submissions to health authorities like the FDA or EMA. To excel in Clinical Project Manager jobs, individuals typically possess a strong educational foundation, usually a bachelor’s or advanced degree in life sciences, nursing, pharmacy, or a related field. Several years of direct experience in clinical research, often within a pharmaceutical company, biotech firm, or CRO, are essential. This experience typically encompasses hands-on work in phases II-III of clinical development. Key skills include exceptional project management and organizational abilities, a keen eye for detail, and superior communication and leadership talents to guide diverse teams. A deep understanding of Good Clinical Practice (GCP), ICH guidelines, and the global regulatory landscape is mandatory. Proficiency in budget management, risk assessment, and problem-solving is also critical. Fluency in English is commonly required for international studies. For those seeking a dynamic career where scientific expertise meets strategic leadership, Clinical Project Manager jobs offer a challenging and impactful pathway. These positions are ideal for professionals dedicated to improving patient outcomes by seamlessly translating scientific hypotheses into robust clinical evidence.

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