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Key Responsibilities:

Study Planning and Design:

  1. Develop detailed study plans, protocols, and objectives in collaboration with stakeholders.
  2. Identify study goals, timelines, and resource requirements.
  3. Coordinate with regulatory bodies to ensure compliance with guidelines and approvals.

Budget and Resource Management:

  1. Prepare study budgets and monitor expenses to ensure cost-effectiveness.
  2. Allocate resources effectively, including personnel, facilities, and equipment.
  3. Manage contracts and agreements with vendors, partners, or external consultants.

Team Coordination:

  1. Lead and oversee study teams, including researchers, data managers, and field personnel.
  2. Provide training, guidance, and support to team members to ensure smooth study operations.
  3. Foster collaboration and communication across multidisciplinary teams.

Study Execution and Monitoring:

  1. Ensure the study is conducted according to protocols, timelines, and quality standards.
  2. Monitor study progress, identify potential risks, and implement corrective actions.
  3. Conduct regular site visits or meetings to review data collection and adherence to guidelines.

Data Management and Analysis:

  1. Oversee the collection, validation, and storage of study data.
  2. Ensure data quality and integrity through audits and checks.
  3. Collaborate with analysts or statisticians to interpret study findings.

Regulatory Compliance and Reporting:

  1. Ensure compliance with ethical standards, laws, and regulations applicable to the study.
  2. Prepare and submit periodic reports to stakeholders, sponsors, and regulatory bodies.
  3. Maintain accurate records and documentation for audits or inspections.

Communication and Stakeholder Management:

  1. Serve as the primary point of contact for sponsors, partners, and stakeholders.
  2. Provide regular updates on study progress, milestones, and outcomes.
  3. Present findings and results in reports, presentations, or publications.

Qualifications:

  • Bachelor’s degree in a relevant field (e.g., science, business, or project management); a Master’s degree or higher is often preferred.
  • Previous experience in study management, project management, or research coordination.
  • Certifications such as PMP (Project Management Professional) or CRA (Clinical Research Associate) are an advantage for clinical settings.

Key Skills:

  • Strong project management and organizational abilities.
  • Excellent communication and leadership skills.
  • Analytical and problem-solving capabilities.
  • Familiarity with research methods, protocols, and regulatory requirements.
  • Proficiency in data management systems and software.



Salary

Competitive

Monthly based

Location

Accra, Greater Accra Region, Ghana

Job Overview
Job Posted:
1 day ago
Job Expire:
17h 51m
Job Type
Full Time
Job Role
Education
Bachelor Degree
Experience
2- 3 Years
Slots...
1

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Location

Accra, Greater Accra Region, Ghana