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Job Offer: Clinical Trial Coordinator:Job description:
Clinical Trial CoordinatorJob location:Auckland All Auckland Work Type: Permanent » » » »Large charitable organisation – South Auckland (close to transport) »Very supportive organization, growth opportunities »Full training, top income, Monday to Friday 40hours (with eg: 3.30pm finish) The Organisation Our client is a large charitable trust that undertakes, promotes, advances and funds research, audit, evidence-located practice and education; high quality and safe pharmaceutical therapies through clinical trial research being their aim. advantages: • Competitive income (way more than any other research organizations) • 6 weeks annual leave • Wellness programmes • A certain amount towards educational fund • Christmas and New year shut down • No weekends, no on-calls, no shift work The Position IMPLEMENTATION OF A COMMERCIAL AND INVESTIGATOR INITIATED CLINICAL TRIAL (IICT), AND MANAGE CLINICAL TRIAL PARTICIPANTS • Actively assist with the start-up documentation of obtaining significant signature for the Clinical Trial documents under the direct guidance of the Research Operations Manager (ROM), Business Manager (BM), Associate Research Manager (ARM), or Grants Manager (GM). • Create source documents for the Clinical Trial. • Create and manage the site file for the Clinical Trial in file management. • Actively participates in all activities leading up to Site Initiation and trial commencement. • Maintain an informed consent log for each participant • Book and co-ordinate clinical trial participants’ clinic appointments within trial specific timeframes and participant needs. • Advises the Principle Investigator (PI) of any change in medical conditions of the participant • Co-ordinates, undertakes and reports all protocol-related investigations and questionnaires within specified timeframes and documents that the PI has been informed of the changes • Ensures secure storage of all study devices on site and maintenance of device accountcapability logs. • Co-ordinates with the Research Nurse who obtains blood and urine samples as specified in the protocol and prepares samples for shipment ensuring that documentation at all stages of the process is accurate and complete. • Ensures all documentation is complete from the development of source documentation, continual maintenance of trial master file, completion of all required CRFs/eCRFs, documentation of Monitor (CRA) and Sponsor personnel visits to site and documentation of close-out and archiving procedures. • There will also be financial management related to clinical trials- example assisting in the development of a clinical trial budget etc. You • Previous research trial co- ordination practice • Knowledge of legal and ethical responsibilities. • Knowledge of medical terminology, anatomy and physiology • Excellent communication still • Attention to detail • capability to work independently and as part of a wider team • Problem solving expertise. • capability to apply common sense/knowledge to carry out instruction furnished in written, oral or diagram form • capability to deal with problems involving several concrete variables in standardised situations • Competent in the use of information technology including Microsoft Office and Outlook. The Package Paid fortnightly, an excellent income is available, plus bonus; a 40 hour week Monday to Friday starting at 7am or 8am (example a 3.30pm finish, ideal for school pick-ups?), close proximity to public transport, opportunities for further career advancement, on the job training and orientation as research practice is not required. To be considered for this position, please send an updated resume through to Dee Das by clicking apply now. Ph 022 657 9248, email- dee@kinetic.co.nz Reference Number: 56123 Contact info: Dee Das Profession: Healthcare & Medical > Clinical Employer : Kinetic Recruitment Date Published: 7/12/2021 1:12:00 PM www.kinetic.co.nz Job location: Auckland All Auckland Work Type: Permanent » » » »Large charitable organisation – South Auckland (close to transport) »Very supportive organization, growth opportunities »Full training, top income, Monday to Friday 40hours (with eg: 3.30pm finish) The Organisation Our client is a large charitable trust that undertakes, promotes, advances and funds research, audit, evidence-located practice and education; high quality and safe pharmaceutical therapies through clinical trial research being their aim. advantages: • Competitive income (way more than any other research organizations) • 6 weeks annual leave • Wellness programmes • A certain amount towards educational fund • Christmas and New year shut down • No weekends, no on-calls, no shift work The Position IMPLEMENTATION OF A COMMERCIAL AND INVESTIGATOR INITIATED CLINICAL TRIAL (IICT), AND MANAGE CLINICAL TRIAL PARTICIPANTS • Actively assist with the start-up documentation of obtaining significant signature for the Clinical Trial documents under the direct guidance of the Research Operations Manager (ROM), Business Manager (BM), Associate Research Manager (ARM), or Grants Manager (GM). • Create source documents for the Clinical Trial. • Create and manage the site file for the Clinical Trial in file management. • Actively participates in all activities leading up to Site Initiation and trial commencement. • Maintain an informed consent log for each participant • Book and co-ordinate clinical trial participants’ clinic appointments within trial specific timeframes and participant needs. • Advises the Principle Investigator (PI) of any change in medical conditions of the participant • Co-ordinates, undertakes and reports all protocol-related investigations and questionnaires within specified timeframes and documents that the PI has been informed of the changes • Ensures secure storage of all study devices on site and maintenance of device accountcapability logs. • Co-ordinates with the Research Nurse who obtains blood and urine samples as specified in the protocol and prepares samples for shipment ensuring that documentation at all stages of the process is accurate and complete. • Ensures all documentation is complete from the development of source documentation, continual maintenance of trial master file, completion of all required CRFs/eCRFs, documentation of Monitor (CRA) and Sponsor personnel visits to site and documentation of close-out and archiving procedures. • There will also be financial management related to clinical trials- example assisting in the development of a clinical trial budget etc. You • Previous research trial co- ordination practice • Knowledge of legal and ethical responsibilities. • Knowledge of medical terminology, anatomy and physiology • Excellent communication still • Attention to detail • capability to work independently and as part of a wider team • Problem solving expertise. • capability to apply common sense/knowledge to carry out instruction furnished in written, oral or diagram form • capability to deal with problems involving several concrete variables in standardised situations • Competent in the use of information technology including Microsoft Office and Outlook. The Package Paid fortnightly, an excellent income is available, plus bonus; a 40 hour week Monday to Friday starting at 7am or 8am (example a 3.30pm finish, ideal for school pick-ups?), close proximity to public transport, opportunities for further career advancement, on the job training and orientation as research practice is not required. To be considered for this position, please send an updated resume through to Dee Das by clicking apply now. Ph 022 657 9248, email- dee@kinetic.co.nz Reference Number: 56123 Contact info: Dee Das Profession: Healthcare & Medical > Clinical Employer : Kinetic Recruitment Date Published: 7/12/2021 1:12:00 PM Skills:
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