Dave-Gregory Chackery Email & Phone Number

Responsible for coordinating, managing, and overseeing the various aspects of clinical trials, including management of CRAs, and CRA support staff relevant to active clinical programs and associated deliverables, with a thorough understanding of the operational and strategic aspects of the associated projects.

 Assist with site start-up activities, including collection of site personnel documents and with supervision, review of clinical site-specific informed consents.  Ensures compliance with protocol and all regulatory policies, procedures and/or guidelines during clinical studies by training/guidance of investigators/research coordinators, conducting periodic on-site evaluations and follow-up of corrective actions.  Ensures validity of trial information by monitoring and tracking… Show more  Assist with site start-up activities, including collection of site personnel documents and with supervision, review of clinical site-specific informed consents.  Ensures compliance with protocol and all regulatory policies, procedures and/or guidelines during clinical studies by training/guidance of investigators/research coordinators, conducting periodic on-site evaluations and follow-up of corrective actions.  Ensures validity of trial information by monitoring and tracking clinical trial data (CRFs, source documents, diagnostic reports, inventory logs, etc.) to identify/resolve discrepancies and obtain missing data.  Identifies, evaluates, reports and ensures follow-up of adverse experiences by timely and accurate documentation and appropriate communication of all Adverse Event reports per internal procedures and regulatory requirements.  Maintains working knowledge of clinical trial regulations for applicable geographies and types of studies. Serves as a resource related to clinical trial regulations.  Serves as a mentor for new employees.  Ensures timely collection of trial documentation by obtaining, maintaining and controlling all necessary records and documentation according to procedures and regulations.  Ensures proper supply, accountability and storage of investigational product.  Drives trial enrollment and identifies and communications potential and actual obstacles to enrollment.  Ensures adherence to applicable ethical, regulatory, and clinical standards by participating in the creation, review, and approval of departmental operating procedures, code of ethics, and mission statement.  Identifies and evaluates qualified investigators, investigational sites, and CROs.  Attends investigational cases as needed. Develops and maintains knowledge of specific trial therapeutic area and competitive landscape. Show less

New Hamshire

 Organize and manages clinical trials and research studies. Provides expertise and guidance to the research team and investigators Conducts protocol reviews to assess the feasibility of potential studies. Seek new research opportunities. Participate in study site selection activities Prepare and submit regulatory documents to study sponsors and any applicable regulatory agencies Work with study investigators to develop recruitment and screening procedures. Design and develop… Show more  Organize and manages clinical trials and research studies. Provides expertise and guidance to the research team and investigators Conducts protocol reviews to assess the feasibility of potential studies. Seek new research opportunities. Participate in study site selection activities Prepare and submit regulatory documents to study sponsors and any applicable regulatory agencies Work with study investigators to develop recruitment and screening procedures. Design and develop recruitment documentation Compose informed consent forms and protocol abstracts. Create other study documents and study management tools Maintains study and regulatory documentation. Monitor and manages compliance with regulatory requirements for other members of the research team Carry out study visit tasks and procedures. Arrange required tests and other appointments. Interview study participants about their medical history, medications, adverse events, demographics, and quality of life issues Communicate with participants through the course of the study Travel to investigator meetings and study training Provide education and support to study participants and their families Act as liaison between principal investigators, regulatory agencies, Dartmouth-Hitchcock stakeholders, and study participants to resolve problems Participate in the preparation of grants for funding department research Works with others in the financial management of the department’s research Ability to navigate PubMed Design and manage REDCap database for research studies Show less

Toronto, Canada Area

 Participated as an SME on the electronic Anticoagulation Medical System (eAMS) Provided clinical knowledge regarding atrial fibrillation and anticoagulation guidelines Gained indispensable experience in cardiology/hematology focused research Primary author on research article for eAMS Implemented CDSS for atrial fibrillation into Canadian EMRs Developed workflow diagrams, data dictionary, and test cases Interpreted ACCP guidelines on anticoagulation regarding… Show more  Participated as an SME on the electronic Anticoagulation Medical System (eAMS) Provided clinical knowledge regarding atrial fibrillation and anticoagulation guidelines Gained indispensable experience in cardiology/hematology focused research Primary author on research article for eAMS Implemented CDSS for atrial fibrillation into Canadian EMRs Developed workflow diagrams, data dictionary, and test cases Interpreted ACCP guidelines on anticoagulation regarding non-valvular atrial fibrillation Extensive research and interpretation of medical and scientific literature using PubMed Contributed to creating informed consent forms, regulatory documents and study protocols using ICH GCP guidelines Show less

Greater Chicago Area

Clinical rotations in core clinical sciences and electives including:Family Medicine Core Rotation (12/20/10 - 01/28//11, 6 weeks)Internal Medicine Core Rotation (01/31/11 - 04/22/11, 12 weeks)OB/GYN Core Rotation (04/25/11 - 06/03/11, 6 weeks)Pediatrics Core Rotation (06/06/11 - 07/15/11, 6 weeks)Surgery Core Rotation (07/18/11 - 10/07/11, 12 weeks)PM&R Elective Rotation (10/11/11 - 11/04/11, 4 weeks)Psychiatry Core Rotation (11/21/11 - 12/30/11, 6… Show more Clinical rotations in core clinical sciences and electives including:Family Medicine Core Rotation (12/20/10 - 01/28//11, 6 weeks)Internal Medicine Core Rotation (01/31/11 - 04/22/11, 12 weeks)OB/GYN Core Rotation (04/25/11 - 06/03/11, 6 weeks)Pediatrics Core Rotation (06/06/11 - 07/15/11, 6 weeks)Surgery Core Rotation (07/18/11 - 10/07/11, 12 weeks)PM&R Elective Rotation (10/11/11 - 11/04/11, 4 weeks)Psychiatry Core Rotation (11/21/11 - 12/30/11, 6 weeks)Family Medicine Elective Rotation (03/26/12 - 04/20/12, 4 weeks)Addiction Medicine Elective Rotation (10/22/12 - 11/16/12, 4 weeks)Ambulatory Surgery Elective Rotation (11/26/12 - 12/21/12, 4 weeks)Responsibilities included analyzing and interpreting clinical data for effective patient medical management strategy through use of proper medical and pharmaceutical procedure. Performed patient history and physical examinations. Managed patient disease in collaboration with physicians, residents, and nurses. Gained familiarity with hospital management, financial, and administrative structure. Knowledge of HIPPA. Conducted literature searching using medical databases (i.e., PubMed, Ovid, and UpToDate). Show less

Greater Chicago Area

Clinical rotations in elective sciences including:Radiology Elective Rotation (01/16/12 - 02/10/12, 4 weeks)Cardiology Elective Rotation ( 02/27/12 - 03/23/12, 4 weeks)Responsibilities included analyzing and interpreting clinical data for effective patient medical management strategy through use of proper medical and pharmaceutical procedure. Performed patient history and physical examinations. Managed patient disease in collaboration with physicians, residents, and nurses… Show more Clinical rotations in elective sciences including:Radiology Elective Rotation (01/16/12 - 02/10/12, 4 weeks)Cardiology Elective Rotation ( 02/27/12 - 03/23/12, 4 weeks)Responsibilities included analyzing and interpreting clinical data for effective patient medical management strategy through use of proper medical and pharmaceutical procedure. Performed patient history and physical examinations. Managed patient disease in collaboration with physicians, residents, and nurses. Gained familiarity with hospital management, financial, and administrative structure. Show less

Toronto, Canada Area

http://ce.stmikes.utoronto.ca/Responsible for clerical duties, bookkeeping, data entry, organizing classes, coordinating classes, maintain website, prepare course handbook.

Toronto, Canada Area

http://ce.stmikes.utoronto.ca/Worked with students and staff ensuring courses ran smoothly. Ensured supplies, A/V equipment, and refreshments were made available. Collected tuition. Unlock and lock classrooms.

Toronto, Canada Area

Engineer of express train, providing transportation for CNE patrons.

Toronto, Canada Area

Clerical and bookkeeping duties. Prepared weekly payroll.

Toronto, Canada Area

Baked bread, cakes, and pastries. Stocked shelves. Maintain appearance of bakery.

Doctor Of Medicine (M.D.)

Bachelor'S Degree, Life Science

Life Science with major in Biology