Seeks to recruit a motivated individual to drive organizational success by fulfilling key responsibilities and meeting specified requirements. Aims to identify a candidate capable of performing essential duties efficiently while adhering to all outlined expectations. Focuses on attracting a professional who can contribute to team goals through dedicated effort and adherence to job standards.
The Research Officer will oversee the recruitment and enrollment of participants for the study at designated healthcare facilities within Nairobi County. This role will involve direct reporting to the Study Coordinator.
Perform a range of specialized duties and obligations associated with the role, including but not limited to conducting detailed analyses, managing project deliverables, and ensuring adherence to established protocols. Oversee key operational functions by coordinating cross-functional teams, monitoring progress against milestones, and implementing corrective measures as necessary. Maintain compliance with industry standards and regulatory requirements while documenting processes and outcomes with precision. Collaborate with stakeholders to gather input, align objectives, and drive continuous improvement initiatives. Additionally, troubleshoot issues, propose solutions, and contribute to strategic planning efforts to enhance overall efficiency and productivity.
Conducting thorough screening, recruitment, and enrollment of qualified participants in strict adherence to the study’s established guidelines.
Gather information in accordance with the established Standard Operating Procedures to ensure compliance and accuracy.
Data entry duties involve inputting collected information into the Android tablet system using Redcap for accurate and efficient record management.
Ensure the integrity, completeness, and secure handling of collected data while maintaining compliance with study standard operating procedures (SOPs) and adhering to the best clinical practices for proper storage.
Adhere to Google Cloud Platform (GCP) operational protocols and maintain strict confidentiality protocols throughout all duties.
Each day, compile and produce comprehensive summaries detailing the screened and enrolled study participants in the clinical study.
The study participants must receive the correct interventions and procedures as part of the study protocol.
Compliance with study procedures by participants must be diligently ensured throughout the duration of the research.
To effectively interpret and apply the study Standard Operating Procedures (SOPs) with precision, ensuring compliance with established protocols and guidelines throughout the research process.
Maintain strict adherence to the study procedures’ Standard Operating Procedures (SOPs) throughout the duration of the study.
Provide comprehensive instruction to the facility staff on the PM+ system to ensure they are proficient in its operation and maintenance.
Prepare and submit biweekly reports detailing recruitment activities and participant enrollment for the study to the study Coordinator.
Monthly, complete data capture forms to document modifications in study strategies.
We’re seeking a highly motivated individual with a strong background in [industry/field] to join our team. The ideal candidate will possess at least [X] years of experience in [specific role or skill], proficiency in [software/tool], and a proven track record of [specific achievement]. You should have excellent communication skills, both written and verbal, and the ability to collaborate effectively with cross-functional teams. Additionally, you must be able to work independently, manage multiple priorities, and meet tight deadlines while maintaining a high level of accuracy and attention to detail. Familiarity with [specific industry standard or regulation] is a must, along with the ability to analyze complex data and make informed decisions.
A recognized institution must confer a Diploma in Community Health, Social Work, or Counselling Psychology.
Fluency in both English and Kiswahili—widely spoken languages among our research participants—is essential.
Minimum of two years of research experience is required.
Requires strong proficiency in utilizing REDCAP for data collection purposes.
A strong familiarity with the study area, specifically Nairobi County, is essential for this role.
We require strong proficiency in computer applications and systems.
Certified proficiency in Good Clinical Practice and Human Subjects Protection with a validity extending through the next 48 months from the publication date of this announcement is an essential requirement.
Must possess strong communication abilities, including the capacity to engage consistently with the study coordinator through email and Zoom.
Skilled collaborator adept at engaging constructively with fellow study personnel at the research location.
If you meet the qualifications for the position, kindly submit the aforementioned documents to breakthroughprogram2024@gmail.com by June 8, 2026.
Qualifications
Diploma
Experience Required
2 years
