BFT Clinical Research Project Manager needed for Men27s Health at BWH
BFT Clinical Research Project Manager needed for Men27s Health at BWH
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Salary Not Disclosed
1 Vacancy
Job Description
B.S. Required M.S.preferred.
Minimum 5 yearsof progressively more responsible clinical research experience.
Prior supervisoryexperience required.
Must possess theability to work independently and display initiative to introduce innovationsto research study.
Must have soundinterpersonal skills and the ability to supervise others.
Must possessstrong analytical skills and conceptual thinking.
Excellent oraland written communication skills.
Ability toprioritize tasks and set deadlines.
Ability toidentify problems and develop solutions.
High degree ofcomputer literacy.
Ability to demonstrateprofessionalism and respectfor subjects rights and individual needs.
Mustobtain and maintain certification for Protection of Human Subjects and GCP.
This position will workvery independently with guidance from the Operations Director and/or PrincipalInvestigator (PI) on the Prostate Cancer (PC) clinical study in the MensHealth Unit. S/He will coordinate allactivities of research including but not limited to: subject recruitmentefforts subject study visits IRB protocol development protocol amendmentsand protocol deviation reporting and other regulatory responsibilities supervising the dailyactivities of research at the clinical trialsite at Johns Hopkins implementing and maintaining quality assuranceprocedures performing statistical analyses.
1.In collaborationwith the Operations Director and or PI develops implements and/or maintains anorientation and training program for all staff related to the PC study.
2.May coordinateall (or portion) of research study activities.Function as a resource for all study issues. Identifies problems and develops solutions.This includes acting as lead coordinator on this complicated trial.
3.Designsimplements and evaluates recruitment strategies for study participants at boththe BWH and Johns Hopkins sites.
4.Interact withpatients/subjects with regard to study including patient education proceduralinstruction followup. May serve as aliaison between patient and physician.
5.Responsible foroverseeing the data collection process.Ensures integrity of patient data.
6.Implements andmaintains quality assurance procedures and systems.
7.Plans designsand performs statistical analyses.
8.In collaborationwith PI prepares and may present certain portions of presentations inaddition to preparing articles for publication.
9.Maybe responsible to monitor study budget in collaboration with theAdministrative Director.
10.Hasmanagement responsibility for study personnel involved in the PC studyincluding hiring evaluation orientation and training.
11.Servesas the primary contact for outside vendors utilized to ensure efficient operationsof the study.
12.Ona daily basis executes the procedural managerial and policy decisions madefor the study.
13.Allother duties as assigned.
Required Experience:
IC
Employment Type
Full-Time
