Job Opportunities

Sr. Clinical Project Managers are Responsible for:

All aspects of project administration and coordination of multiple large-scale, multi-center clinical trials.  This includes the review of all proposals, budgets and contracts and tracking of all milestones and timelines.  Assumes the responsibility for bigger trials both in number and complexity than other Project Managers.  The development of study related documents and overall direction of the clinical sites for protocol adherence is under the direction of the Project Manager.  Independent decision making based upon current factors related to specifics of each clinical trial is required.  The incumbent is responsible and accountable for assuring that the project team that he/she leads meets all deadlines and is also required to maintain a close effectual working relationship with Sponsors, Research Coordinators and Principal Investigators.  Manages other personnel both directly and indirectly.  Mentors all other Project Managers in the conduct of clinical trials.  Must be willing to serve on internal committees.  Serves as a mentor to new Project Managers. 

Primary Duties:

1.       Manage interdisciplinary team                                                                                             

2.       Review proposals, budgets and contracts                                                                             

3.       Create timelines                                                                                                                 

4.       Track milestones                                                                                                    

5.       Facilitate all internal and external communication                                                      

6.       Mentor Project Managers                                                                                                   

7.       CRF/MOP development                                                                                         

 8.       Supervise subcontractors                                                                            

9.       Investigator meetings/Site initiations

10.     Strong Management skills 

Secondary Duties:

1.       Coordinate DSMB’s

2.       Oversight of data submissions

3.       Coordination of data requests

4.       Supervises development of reports

5.       Review of reports

6.   Assist with the development of departmental processes

Supervises and directs a Project Team consisting of a Database Manager, Nurse Reviewer,

Biostatistician, Programmer, Safety  and ancillary personnel needed to conduct a clinical trial. 

These positions report to their own department heads.  Project Managers are involved in the interviewing process.  

Is the primary mentor/trainer for all new Project Managers. Supervises at least one Admin and/or Research Assistant. 

Prepares and delivers annual performance reviews on these individuals. 

Requirements:

Education:

Required: Masters (completed or in progress), or equivalent professional experience

Preferred:  Masters plus Project Management Training 

Yrs. of related experience:

Required: 6+, clinical trial mgmt.

Preferred: 2-5 yrs HCRI experience  

Travel:  Investigator meetings, site initiation meetings, professional conferences