Oversee and execute a range of critical duties, ensuring alignment with organizational objectives and industry standards. Implement and maintain processes that enhance efficiency, productivity, and quality across all assigned functions. Collaborate with cross-functional teams to drive project success, resolve challenges, and foster innovation. Monitor performance metrics and key indicators to identify trends, mitigate risks, and optimize outcomes. Provide leadership and mentorship to team members, promoting professional growth and accountability. Ensure compliance with relevant policies, regulations, and best practices to uphold organizational integrity.
Conduct thorough screening, obtain informed consent, and register study participants who fulfill specified eligibility requirements while strictly upholding ethical standards and study protocols.
Conduct initial and subsequent physical assessments, delivering standard clinical services such as daily ward visits for study participants.
Administer the investigational product safely by strictly adhering to the study protocol’s approved guidelines.
Diagnose and oversee incidental illnesses, ensuring continuous monitoring, detailed documentation, and timely reporting of any adverse reactions associated with the investigational product.
Assess participants for admission, ongoing care, or referral in alignment with the study protocol, ensuring well-informed clinical decisions.
Examine study questionnaires thoroughly to verify the precision, thoroughness, and uniformity of the data prior to entry.
Compile and deliver comprehensive weekly and monthly reports detailing clinic operations, such as enrollment figures, exclusion data, exclusion rationales, and follow-up strategies.
Track participant visits meticulously, documenting both initial and subsequent appointments to assess progress and confirm adherence to clinic schedules.
Collect, organize, and document biological specimens while maintaining strict adherence to proper handling protocols and ensuring their prompt delivery to the laboratory. Additionally, assist in monitoring and supporting laboratory operations to maintain efficiency and accuracy throughout the process.
Perform verbal autopsies for community deaths that occur outside healthcare facilities to guarantee thorough and precise reporting of causes and circumstances.
Oversee inventory and stock levels to ensure sufficient and systematically arranged supplies are available at the study site.
Assist with various other tasks as directed by management to ensure comprehensive support and operational efficiency.
Vacancy Requirements:
Mandatory qualification includes a Diploma in Clinical Medicine & Surgery.
A minimum of three years of hands-on experience in clinical research or within a high-volume clinical environment is required.
A current registration certificate and a valid professional practicing license from the applicable regulatory authority are essential requirements.
Individuals with prior involvement in clinical trials will be given preferential consideration.
Proficiency in clinical trial methodologies offers a distinct advantage, while participation in such trials is essential.
Skilled in utilizing a variety of computer applications, such as Microsoft Word, Excel, PowerPoint, Zoom, and email communication platforms, with proficiency being a requirement.
Able to handle numerous responsibilities simultaneously while effectively prioritizing tasks in a high-pressure setting.
Proven ability to collaborate seamlessly within cross-functional teams, consistently delivering value to collective objectives.
To apply, please submit your application through the designated method as outlined in the job posting. This may include completing an online application form, sending your resume and cover letter via email, or utilizing a company portal. Ensure all required documents and information are provided accurately to facilitate the review process. If you have any questions regarding the application method, feel free to reach out to the hiring team for clarification.
To initiate your application, please access the link(s) provided below via the company’s official website.
Qualifications
Diploma
Experience Required
3 years
