Principal Investigator

Further your career in research with Genge Partners

For Patients:

  • Offer cutting-edges life-altering treatment options

  • Improve health outcomes and quality of care

  • Early (pre-approval) access to innovative care & therapies

  • Direct medical and nursing care

For the Doctor

  • Earn additional revenue

  • Increase visibility with the drug development sector in the pharmaceutical industry

  • Imbedded administrative and nursing support

Build your research program with Genge Partners:

Our Goal is to Facilitate and expedite research by breaking down barriers.

 

Grow your research at no cost with GP?

The main responsibility of the PI of a clinical trial is to oversee the clinical trial and to ensure the trial is conducted according to the investigational plan and applicable regulations according to FDA 21 CFR 312.60 and Health Canada.

Genge Partners assists the PI by having dedicated personnel to take care of the administrative, financial, and operational activities of a clinical trial this includes but not limited to:  

    • Facilitate sponsor site visits and monitoring

    • Complete sponsor required forms and correspondence 

    • Provide regulatory guidance and oversite

    • Preparations for audits and inspections

    • Ethics Board submissions

    • Regulatory binder maintenance

    • Coordination of third-party payments

    • Contract and budget negotiations

    • Invoicing and payment reconciliation

    • Coordination of study closure activities

    • Archiving of study documents and records

    • Assist with training and GCP documentation

    • Annual review of all necessary certifications are up to date and assist with completion if any are expired

    • Assist with updating CVs

    • Support for grant writing and funding applications

    • Provide guidance and review financial disclosures and conflict of interest forms

    • Assist with documentation of investigator oversite:

    • SAE Reports

    • Eligibility checklists

    • Review of CRA/Monitor visit letters

    • Review of abnormal lab results

 

The New Model:

The Genge Partners model utilizes a bottom-up model to develop a truly efficient organization to deliver quality data in a timely manner while not overextending resources.

 

Trusted Resource :

Leveraging a trusted –world-renowned reputation as a clinical trial partner with pharma, CROs, and various Pan-Canadian and international networks

Knoweldgeable:

Leveraging knowledge of best practices and coordinator expertise to ensure efficiency to adapt to multiple therapeutic areas and is scalable to match any recruitment targets and/or study complexity 

Quality Assured:

All aspects of trial execution including data management meet industry standards for compliance, accountability, regulatory requirements 

Genge Partners Director Dr Angela Genge: ​

Dr Angela Genge has been a clinical trialist since 1990, she became PI in clinical trials when she began as an attending physician at the Montreal institute in 1994, she has participated in over 400 clinical trials as a PI, sub-I, or rater.

Submit your CV

We invite you to send us your CV so that we can review it and contact you if we have a job opening that matches your profile.