Clinical Operations Manager handling clinical trial budgets and negotiations in Poland. Contributing to patient health improvements through clinical research solutions.
PA
Parexel
Currently Hiring
About the company
Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster.
Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere.
Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient.
With the people, insight and focus on operational excellence, we work With HeartTM every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference.
For more information, visit parexel.com.
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Open jobs
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15 jobs found
Senior Regulatory Affairs Consultant at Parexel developing regulatory submission strategies for pharmaceutical products. Leading regulatory teams and managing multiple submissions in a fast - paced environment.
Project Manager overseeing complex Research & Development pharma projects at Parexel. Involves project initiation, planning, risk management, and documentation responsibilities.
Senior Regulatory Affairs Associate developing artwork strategies for Parexel's global product portfolio. Ensure compliance and manage labeling governance for EU, US, and ROW markets.
Solicitor providing legal advice and negotiating contracts for Parexel's global operations. Requires strong experience in commercial law and collaboration skills.
(Senior) Regulatory Affairs Consultant managing regulatory submissions for various clients at Parexel. Collaborating with stakeholders and ensuring high - quality work for client satisfaction.
Principal Scientist I or II at Parexel providing operational support for chemistry sourcing projects and ensuring high - quality delivery of products and services.
Regulatory Affairs Consultant providing regulatory input for EU product labelling and promotional materials. Collaborating with cross - functional teams in various European locations.
Clinical Research Associate engaging with clinical sites and managing trial quality for Parexel's biopharmaceutical services. Ensuring patient safety and compliance with regulatory protocols across designated clinical trials.
Clinical Study Administrator assisting in the coordination and administration of study activities. Joining Parexel to improve global health through clinical trials and regulatory consulting.
Senior Clinical Study Administrator coordinating clinical studies for leading biotechs at Parexel. Involves administration, document management, and regulatory compliance in a hybrid role.
Senior AI Solution Developer leveraging Palantir Foundry to create AI - driven solutions for Parexel's business. Collaborating with teams to develop innovative ML solutions and applications.