17.2 C
New York
Friday, April 19, 2024
More

    Latest Posts

    Site Coordinator at KCCR KUMASI


    October 19th, 2020 at 04:54 pm

    The post-holder shall undertake various activities associated with the research groups. These activities will be performed at the Komfo Anokye Teaching Hospital, Kumasi, Ashanti Region, Ghana. The post-holder is expected to have good organisational and communication skills. He/She should be willing to work efficiently within a multidisciplinary team in order to perform all activities in a timely fashion.

    1. Functional Relationships

    The Site Coordinator is part of a team consisting of international and local investigators. The Site Coordinator serves as a liaison between the research group and KCCR administrative department; and between KCCR and the institute partners within the consortia the research group belong to. The Site-Coordinator is accountable to the local Principal Investigators (PIs). The Site Coordinator should always maintain a good relationship with the co-worker, KCCR staff and the external partners by communicating in a professional and courteous manner. The Site-Coordinator with work closely with the Field Coordinator.

    1. Scope of the Position

    The Site Coordinator oversees the project activities to ensure the desired results are achieved by providing administrative and financial support to a portfolio of in-country and multi-country projects and working closely with the PIs, the Project Finance Officer, partner institutions, KCCR finance and administrative departments and ensuring compliance with funders’ policies.

    The Site-Coordinator put in place a structure that optimized the efficiency of the communication and administrative process for the research team.

    1. Tasks and Responsibilities

    Communication

    –          Facilitate the relationship between the PIs, the Lead Institution and the Funders.

    –          Manage internal and external communication with partner institutions.

    Planning of resources

    –          Plan with the PIs on the sourcing and use of resources to achieve the goals and objectives of the projects within allotted timelines and budgets.

    –          Coordinate the planning, preparation and submission of grant applications.

    Monitoring Progress and Risks Management

    –          Monitor the preparation and progress of each milestone and deliverables of the projects. Ensure that progress are made in time with the deadlines assigned to enable the projects to run smoothly.

    –          Oversee regulatory compliance issue regarding Clinical Trials and record Institutional Review Board approvals.

    –          Manage administrative aspects of the projects in line with funders’ requirements.

    –          Perform day-to-day management of project team and address any team issues promptly in consultation with the PI(s).

    –          Conduct regular meetings with the local team and also with partner institutions to discuss project status and issues in a transparent manner.

    Reporting and Documentation

    –          Organize, support, provide follow-up and report pertinent issues to PIs.

    –          Prepare project documents and research reports for PIs.

    –          Represent PIs in a meeting if necessary.

    –          Prepare annual technical reports to grantors.

    1. Required qualifications, competences and experience

    Qualifications:

    –          Master’s or higher degrees

    –          At least 2 years of experience in project management, including within international Consortia or Research Networks

    Essential attributes

    –           Excellent written and oral communication skills in English

    –       Dynamic person with demonstrated capacity for team work and team leadership

    –       Critical thinking, excellent analytical abilities and attention to detail

    –       Familiar with clinical research activities

    –       Ability to prioritize workload, assume responsibility for work, and follow through to completion

    –       Ability and willingness to work under pressure as a part of a global team

    –       High computer literacy including knowledge of Microsoft software products, Office suites, management software etc.

    Desired Attributes

    –          Familiarized with Good Clinical Practice (GCP)

    –          Oral and written proficiency in French

    1. Remuneration

    Remuneration will be according to KCCR standards. The contract will be for 12-months (renewable), with the first 3 months as probation.

    1. How to apply

    Email the following to: the Head of Administration, KCCR, KNUST, (e-mail: [email protected] and copy [email protected]) no later than October 21, 2020,17:00 GMT.

    –    A motivation letter (350 words)

    –    A detailed CV including the contact numbers and/or email addresses of three referees

    –    Two recommendation letters

    Expected starting date: November 1, 2020

    Latest Posts

    spot_imgspot_img

    Don't Miss

    Stay in touch

    To be updated with all the latest news, offers and special announcements.