better Research Development Job at PharmaNet Inc

Assist in managing large scale clinical trial projects or function as project manager for small scale projects, ensuring on-time, on-budget performance Monitor (pre-study, initiation, routine, and close-out visits) investigator sites for GCP compliance according to PharmaNet SOPs and/or client guidelines Recruit investigators Negotiate study budgets with investigators Obtain, review, and process regulatory and administrative documents from investigator sites Review and develop protocols Review and

Assist in managing large scale clinical trial projects or function as project manager for small scale projects, ensuring on-time, on-budget performance Monitor (pre-study, initiation, routine, and close-out visits) investigator sites for GCP compliance according to PharmaNet SOPs and/or client guidelines Recruit investigators Negotiate study budgets with investigators Obtain, review, and process regulatory and administrative documents from investigator sites Review and develop protocols Review and

Assist in managing large scale clinical trial projects or function as project manager for small scale projects, ensuring on-time, on-budget performance Monitor (pre-study, initiation, routine, and close-out visits) investigator sites for GCP compliance according to PharmaNet SOPs and/or client guidelines Recruit investigators Negotiate study budgets with investigators Obtain, review, and process regulatory and administrative documents from investigator sites Review and develop protocols Review and develop

Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites (40 50% travel) for GCP compliance according to PharmaNet SOPs and/or client guidelines Recruit investigators for participation in clinical trials Negotiate study budgets with investigators Obtain, review for appropriateness, and process regulatory and administrative documents from investigator sites Review draft protocols for completeness and feasibility Develop Case Report Forms for clinical trials Present (e.g

Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites (40 50% travel) for GCP compliance according to PharmaNet SOPs and/or client guidelines Recruit investigators for participation in clinical trials Negotiate study budgets with investigators Obtain, review for appropriateness, and process regulatory and administrative documents from investigator sites Review draft protocols for completeness and feasibility Develop Case Report Forms for clinical trials Present (e.g

Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites (40 50% travel) for GCP compliance according to PharmaNet SOPs and/or client guidelines Recruit investigators for participation in clinical trials Negotiate study budgets with investigators Obtain, review for appropriateness, and process regulatory and administrative documents from investigator sites Develop Case Report Forms for clinical trials Present (e.g. study specific guidelines and procedures, case report forms

Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites (40 50% travel) for GCP compliance according to PharmaNet SOPs and/or client guidelines Recruit investigators for participation in clinical trials Obtain, review for appropriateness, and process regulatory and administrative documents from investigator sites Review draft protocols for completeness and feasibility Develop Case Report Forms for clinical trials Present (e.g. study specific guidelines and procedures, case

Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites (40 50% travel) for GCP compliance according to PharmaNet SOPs and/or client guidelines Recruit investigators for participation in clinical trials Negotiate study budgets with investigators Obtain, review for appropriateness, and process regulatory and administrative documents from investigator sites Review draft protocols for completeness and feasibility Develop Case Report Forms for clinical trials Present (e.g

Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites (40 50% travel) for GCP compliance according to PharmaNet SOPs and/or client guidelines Recruit investigators for participation in clinical trials Negotiate study budgets with investigators Obtain, review for appropriateness, and process regulatory and administrative documents from investigator sites Review draft protocols for completeness and feasibility Develop Case Report Forms for clinical trials Present (e.g

We currently have openings for Regional, home-based Clinical Research Associates throughout the United States. Monitor (pre-study, initiation, routine, and close-out visits) at investigator sites (up to 80% travel) for GCP compliance according to PharmaNet SOPs and/or client guidelines Generate study specific documentation including monitoring trip reports, telephone contact reports, site correspondence, and expense reports. Recruit investigators for participation in clinical trials Conduct project feasibility

Assist in managing large scale clinical trial projects or function as project manager for small scale projects, ensuring on-time, on-budget performance Monitor (pre-study, initiation, routine, and close-out visits) investigator sites for GCP compliance according to PharmaNet SOPs and/or client guidelines Recruit investigators Negotiate study budgets with investigators Obtain, review, and process regulatory and administrative documents from investigator sites Review and develop protocols Review and

Assist in managing large scale clinical trial projects or function as project manager for small scale projects, ensuring on-time, on-budget performance Monitor (pre-study, initiation, routine, and close-out visits) investigator sites for GCP compliance according to PharmaNet SOPs and/or client guidelines Recruit investigators Negotiate study budgets with investigators Obtain, review, and process regulatory and administrative documents from investigator sites Review and develop protocols Review and