Jobs at IQVIA | MyJobMag (2024)

Posted: Jul 27, 2024

Deadline: Not specified

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• We are looking for a Consultant in Kenya who will join an exciting working environment in a dynamic and international atmosphere.

Responsibilities:
After a massive and never-ending training, you will be ready to:

• Increase efficiency in the management of the stroke patients
• Support hospitals and healthcare professionals with continuous training and organizational tools
• Be an expert Therapeutic Consultant promoting new diagnostic and treatment guidelines to hospitals
• Foster and promote quality monitoring programs to keep consistent hospital performance
• Extend the reach of project to new hospitals
• Lead the multidisciplinary stroke teams through continuous improvement
• Improve therapeutic protocols in the major hospitals

Required Skills:

• Excellent Scientific Background
• Ideally PhD in Neuroscience
• High motivation and very good people skills
• Fluency in English
• Leadership skills
• Proactivity, flexibility and problem solving’ skills
• Availability to travel up to 70% of the time

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Job Overview

• Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

Essential Functions

• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
• Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
• Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
• Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
• Collaborate and liaise with study team members for project execution support as appropriate.
• If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
• If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.

Qualifications

• Bachelor's Degree Degree in scientific discipline or health care preferred.
• Requires at least 2 years of year of on-site monitoring experience.
• Equivalent combination of education, training and experience may be accepted in lieu of degree.
• Good knowledge of, and skill in applying, applicable clinical research regulatory requirements, i.e. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Good therapeutic and protocol knowledge as provided in company training.
• Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
• Written and verbal communication skills including good command of English language.
• Organizational and problem-solving skills.
• Effective time and financial management skills.
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

Use the link(s) below to apply on company website.

• Medical Science Liaison - Kenya
• Senior Clinical Research Associate

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