Orano Med, LLC.
Senior Clinical Project Manager
Orano Med, LLC., Boston, Massachusetts, us, 02298
Orano Med:Orano Med has developed new processes for producing high-purity lead-212, a rare radioactive isotope. Lead-212 is currently at the heart of promising research projects in nuclear medicine to develop new treatments against cancer. The innovative approach, known as targeted alpha therapy (TAT), recognizes and destroys cancer cells while limiting the impact on nearby healthy cells.Position Summary:
The Senior Clinical Project Manager is responsible for project management and oversight of assigned clinical trials.Position Responsibilities:
Oversight checks including monitoring report review and TMF checks.Status meeting attendance, meeting minute review/taking.Invoice review, confirmation of services received.Support CRO with site level issues including non-compliance, etc.Review data cleaning metrics, address backlogs.Review or create/amend study level documents including ICFs, protocols, study plans, training materials, etc.Provide study status updates.Manage study to budget and timelines.Other duties as assigned.Our Full-Time Benefits
Competitive compensationHealth, Dental, and Vision insurance - with generous employer contributions401(k) with employer matching and contribution amountsLife insurance and Short- and Long-Term Disability insurance provided by the companyGenerous Paid Time Off and holiday schedulesNumerous Training and Development opportunitiesand more...Ideal Qualifications
All candidates must meet the following minimum requirements in order to be considered for this opportunity. Candidates who exceed minimum qualifications may be considered for a higher level position.Minimum Qualifications:
Bachelor's degree in life/physical sciences or nursing.10-12 years, with at least 3 years of experience as a CTM / Clinical Trial Project Manager.Differentiating Qualifications:
Previous experience working with a CRO.Skills/Knowledge:
Knowledgeable in ICH GCP, applicable US regulations, project management and clinical operations, study budgets and timelines.Knowledgeable on platforms including Medidata RAVE, clinical trial management systems, excel, etc.Orano is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, national origin, age, disability, citizenship, veteran status, marital status, sexual orientation, gender identity, genetic predisposition or carrier status or any other characteristic protected by law.
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The Senior Clinical Project Manager is responsible for project management and oversight of assigned clinical trials.Position Responsibilities:
Oversight checks including monitoring report review and TMF checks.Status meeting attendance, meeting minute review/taking.Invoice review, confirmation of services received.Support CRO with site level issues including non-compliance, etc.Review data cleaning metrics, address backlogs.Review or create/amend study level documents including ICFs, protocols, study plans, training materials, etc.Provide study status updates.Manage study to budget and timelines.Other duties as assigned.Our Full-Time Benefits
Competitive compensationHealth, Dental, and Vision insurance - with generous employer contributions401(k) with employer matching and contribution amountsLife insurance and Short- and Long-Term Disability insurance provided by the companyGenerous Paid Time Off and holiday schedulesNumerous Training and Development opportunitiesand more...Ideal Qualifications
All candidates must meet the following minimum requirements in order to be considered for this opportunity. Candidates who exceed minimum qualifications may be considered for a higher level position.Minimum Qualifications:
Bachelor's degree in life/physical sciences or nursing.10-12 years, with at least 3 years of experience as a CTM / Clinical Trial Project Manager.Differentiating Qualifications:
Previous experience working with a CRO.Skills/Knowledge:
Knowledgeable in ICH GCP, applicable US regulations, project management and clinical operations, study budgets and timelines.Knowledgeable on platforms including Medidata RAVE, clinical trial management systems, excel, etc.Orano is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, national origin, age, disability, citizenship, veteran status, marital status, sexual orientation, gender identity, genetic predisposition or carrier status or any other characteristic protected by law.
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