Jummy Kilo

About Jummy Kilo

A dedicated Clinical Research Associate with focus on oncology but experienced in medical device also. A strong team player, self-motivated, disciplined, strong verbal and written communication skills, adaptable to various roles. A Certified Clinical Research Project Manager and PMP Project Manager with experience in, information technology, software development and Program management.

Experience

1. Snr Cra

   Parexel

   Nov 2021 — Present · US

   Clinical sites’ main point of contact, accountable for quality and delivery of sites from Initiation to Close out of the trial. Oversees the conduct of the trial at designated sites ensuring the rights and well-being of human subjects are protected, quality and integrity of the reported data and the conduct of the trial is in compliance with the currently approved protocol/amendment(s), with GCP and with the applicable regulatory requirement(s).• Build relationships with investigators and site staff. • Facilitate and support site with access to relevant study systems and ensure sites are compliant with project specific training requirements. • Address and resolve issues at sites, including, questions, potential deficiencies in documentation, communication, and the need for additional training.• Apply working knowledge and judgment to identify and evaluate potential data quality issues. Determine and implement appropriate follow-up action with the input of other / relevant parties and / or guidance provided, if applicable.• Actively participate in Investigator and other external or internal meetings and audits & regulatory inspections as required. • Collect, review, and approve (if applicable) updated/amended site documentation, including regulatory documents as applicable.• Review site recruitment plan in collaboration with the site staff. • Perform and report on-site visits and remote contacts in accordance with the monitoring plan; • Assess & manage test article/study supply including supply, accountability and destruction/return status. • Review & follow-up site payment status. • Follow-up on CRF data entry, query status, and SAEs.• Conduct on-site study-specific training.• Perform site facilities assessments• Maintains sound working knowledge of and ensure compliance with applicable ICH-GCP Guidelines, international and local regulations, PAREXEL SOPs, other PAREXEL / Sponsor training requirements and study specific procedures, plans and training.

Education

• Chesapeake Bible College & Seminary

  Doctorate Student , Pastoral Clinical Counseling

• Ahmadu Bello University

  Bachelor's degree, Economics

  1977 — 1981

• Chesapeake Bible College & Seminary

  Master's degree, Pastoral Clinical Counseling

  2014 — 2017