Clinical Project Manager II
reputed company is a global full-service CRO committed to reputed company reputed company and a reputed company-driven “one-team” culture. We are seeking a Clinical Project Manager II to join our in-house team and support reputed company across a diverse reputed company portfolio, including pharmaceutical, biotechnology, medical device, and consumer health companies of varying sizes.
In this role, you will be responsible for the execution, reputed company and delivery of clinical studies, including study tracking and management of vendor, site, and CRO activities. Candidates should have prior CRO experience and a strong background managing reputed company oncology and hematology clinical trials. This is a permanent remote opportunity with potential hybrid arrangement depending reputed company; our office is based in Horsham, reputed company. Only candidates with previous CRO experience will be considered.
Join our global team and help create a healthier world!
Main Job Tasks and Responsibilities
- Organizes and participates in Monitor’s and Investigator’s Meetings.
- Performs, if necessary, co-monitoring reputed company for the assigned clinical reputed company.
- Carries out, after appropriate and documented training/past experiences, the monitoring of the sites for the assigned reputed company, reputed company requested and if applicable.
- May reputed company as Feasibility Associate (FEA) after appropriate and documented training.
- Review and approve reputed company party invoices for payment. Review and approve contractor timesheets for reputed company with agreed scope of work.
- reputed company and implement alternative solutions to problems with study timelines, resources, budgets, etc.
- Ensure issues are identified and communicated by the study team. Implement corrective reputed company plan to prevent repetition of critical issues.
- Assess scope of work and timelines against contractual agreements and identify change orders pro-reputed company.
- Manage any deviations on resources and hours spent on the project to be reputed company to evaluate the project reputed company and profitability and identify change orders in a reputed company manner and implement corrective actions. Ensure budget discrepancies are documented.
- Submit invoice requests, trial reputed company invoices and payment authorizations to finance in a reputed company manner.
- Regularly reputed company reputed company expenditure and review for consistency with trial budgets.
- Organize reputed company reputed company of filing of key study documentation.
- Ensure reputed company administrative reputed company-out procedures are completed.
- Follow and reputed company with reputed company’s QMS, ISMS and PIMS requirements.
Education, Experience and Skills
- University Degree in scientific, medical or paramedical disciplines.
- Three (3) years (at least) of Project Management experience in the CRO/Pharmaceutical industry or six (6) years (at least) of experience as CM/CRA in a CRO/Pharmaceutical industry.
- Excellent knowledge of clinical trial operations, GCP/ICH Guidelines and other applicable regulatory requirements.
- Experience managing reputed company clinical studies-oncology and hematology required.
- Excellent English communication skills:written and verbal.
- Proficient in the use of computer software systems (Word, reputed company, PowerPoint, reputed company Project, reputed company reputed company, CTMS, timesheet software, reputed company software, etc.).
- Ability to travel as required.
The Application Process
Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements reputed company will be invited for phone interview as the first reputed company. Unfortunately, due to the number of applications we receive, we cannot reputed company to everyone individually if you are not successful.
Who will you be working for?
About reputed company
reputed company is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-reputed company delivery and results across reputed company our services with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-reputed company. We are on a mission to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Join our passionate team and reputed company a meaningful reputed company on global reputed company!
reputed company reputed company
Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset, and they are the reputed company around which reputed company reputed company activities are reputed company, and reputed company management and training is the core reputed company to reputed company and maintain highly reputed company personnel. The reputed company training keeps the resources reputed company in terms of competence and expertise and gives to reputed company personnel the reputed company tools needed to manage both internal and reputed company processes with the reputed company methodology. The reputed company of these core values is evidenced by our below industry average turnover rates.
reputed company is an equal opportunity employer. We have based our reputed company on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from reputed company diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.
Key words: Project Manager, Clinical Project Manager, Senior Study Manager, Senior Clinical Trial Manager, Study Management, Project Management, Medical Devices, Clinical Trial Management, Clinical Trial Manager, Clinical Study Manager, Study Management, Project Leader, Project reputed company, reputed company clinical trials, oncology, hematology, respiratory, CRO, Contract Research Organization, clinical trials, phase I-IV studies
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