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PROJECT MANAGER 1-CARDIAC SAFETY SERVICES
Job Field: Security
Location: San Diego, CA
Salary: $Not stated
Location: San Diego, CA
Salary: $Not stated
JOB SUMMARY:
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<tr><td valign="top" width="450"><b>Title: Project Manager 1-Cardiac Safety ServicesLocation: USA-California-San DiegoOther Locations:Quintiles is the only fully integrated Biopharmaceutical services company offering clinical, commercial, consulting and capital solutions worldwide. The Quintiles network of 26,000 engaged professionals in more than 60 countries around the globe works with an unwavering commitment to patients, safety and ethics. Quintiles helps biopharmaceutical companies navigate risk and seize opportunities in an environment where change is constant. We are continuously in search of talent that can help advance our mission. Currently we are seeking a Project Manager I- Cardiac Safety Services. The Project Manager will manage single and full service cardia safety services projects that are both regional and global in scope. The Project Manager will lead the cross functional project teams including operations, data management, biostatistics, medical writing and QA, to ensure quality, on-time and within budget deliverables for primarily Phase I - IV clinical trials thorough QT Studies. Specific responsibilities may include: managing the study timelines, deliverables and risks, working with the client and Business Services to finalize the project budget and scope, serving as primary contact with client to ensure appropriate communication, managing project budget, and participate in internal and external meetings.BS in life sciences or related field including2 years in Project Management environment and 5 years of clinical research or related relevant experience.* Experience in a key CRO/Pharmaceutical operational function, e.g., data management, clinical operations, laboratory, pre-clinical.* Strongly prefer candidates with solid Phase I - IVmanagement experience.* Experience with resource and budget/financial management.* Good written & oral communication skills.* Good client management skills.* Strong computer/technology skills including MS Excel, PowerPoint, and MS Project (or other similar Project Management tools).* Knowledge of clinical study guidelines including FDA, ICH & GCP.* Ideal candidate will have a firm grasp of the clinical trials process.
</tr>
<tr><td valign="top" width="450"><b>Title: Project Manager 1-Cardiac Safety ServicesLocation: USA-California-San DiegoOther Locations:Quintiles is the only fully integrated Biopharmaceutical services company offering clinical, commercial, consulting and capital solutions worldwide. The Quintiles network of 26,000 engaged professionals in more than 60 countries around the globe works with an unwavering commitment to patients, safety and ethics. Quintiles helps biopharmaceutical companies navigate risk and seize opportunities in an environment where change is constant. We are continuously in search of talent that can help advance our mission. Currently we are seeking a Project Manager I- Cardiac Safety Services. The Project Manager will manage single and full service cardia safety services projects that are both regional and global in scope. The Project Manager will lead the cross functional project teams including operations, data management, biostatistics, medical writing and QA, to ensure quality, on-time and within budget deliverables for primarily Phase I - IV clinical trials thorough QT Studies. Specific responsibilities may include: managing the study timelines, deliverables and risks, working with the client and Business Services to finalize the project budget and scope, serving as primary contact with client to ensure appropriate communication, managing project budget, and participate in internal and external meetings.BS in life sciences or related field including2 years in Project Management environment and 5 years of clinical research or related relevant experience.* Experience in a key CRO/Pharmaceutical operational function, e.g., data management, clinical operations, laboratory, pre-clinical.* Strongly prefer candidates with solid Phase I - IVmanagement experience.* Experience with resource and budget/financial management.* Good written & oral communication skills.* Good client management skills.* Strong computer/technology skills including MS Excel, PowerPoint, and MS Project (or other similar Project Management tools).* Knowledge of clinical study guidelines including FDA, ICH & GCP.* Ideal candidate will have a firm grasp of the clinical trials process.
KEY REQUIREMENTS:
Not stated
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