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Clinical Research Associate /Project Manager - 18537587347

Remote: 
Full Remote
Work from: 

Offer summary

Qualifications:

Fluency in English., Minimum 2 years project management experience in healthcare., Strong team and project management abilities., Proficiency in clinical research methodologies and regulatory requirements., Ability to manage complex schedules and budgets..

Key responsabilities:

  • Lead and manage clinical research projects.
  • Conduct and manage complex research projects.
  • Ensure audit preparedness and regulatory compliance.
  • Attend meetings, recommend policy improvements and collaborate with teams.
  • Track study milestones, invoice sponsors, assist in performance evaluations.
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Somewhere Human Resources, Staffing & Recruiting SME https://somewhere.com/
1001 - 5000 Employees

Job description

Position :             Clinical Research Associate (CRA)/Project Manager (PM)
Working Hours :                                Core work hours are 9 AM - 5 PM PKT, 

Salary Range : 1000 - 1,500 USD


ABOUT THE COMPANY: Our organization operates within a dynamic, international environment, dedicated to advancing clinical research. We foster a collaborative atmosphere where flexibility and adaptability are crucial to engaging effectively with team members and clients worldwide.

ABOUT THE ROLE:

We are seeking a highly motivated and experienced Clinical Research Associate (CRA)/Project Manager (PM) to lead and manage clinical research projects. The ideal candidate will possess a robust background in clinical research and project management, capable of handling complex projects and leading diverse teams effectively.

SCOPE OF WORK:

Project Management:

  • Lead clinical research projects.
  • Design project workflows and charters.
  • Setup projects on OIRRC systems.
  • Develop and maintain project schedules, set targets, and ensure accountability.
  • Lead internal and client meetings, prepare agendas, and approve minutes.

Team Leadership (for leadership positions):

  • Supervise and guide CRAs/PMs.
  • Assist with recruitment.
  • Develop and administer training modules.
  • Mentor junior staff, including hiring and performance evaluations.

Clinical Research:

  • Conduct and manage complex research projects.
  • Oversee large studies or manage smaller studies across multiple sites.
  • Develop systems for data management.

Compliance and Quality Assurance:

  • Adhere to organizational policies and procedures.
  • Ensure audit preparedness and regulatory compliance.
  • Implement corrective actions and processes.
  • Inspect study documents for compliance.

Communication and Collaboration:

  • Attend relevant meetings with sponsors, vendors, and contractors.
  • Be available for emergency calls during off-hours.
  • Recommend and implement policy improvements.
  • Collaborate with cross-functional teams.

Financial Management:

  • Track study milestones and invoice sponsors as per contracts.

Performance Evaluation:

  • Assist in appraising and reviewing the Clinical Operations team's performance.

Continuing Education and Knowledge Sharing:

  • Participate in continuing education and training.
  • Prepare presentations on scholarly articles.
  • Attend virtual conferences and share insights.
  • Contribute to team knowledge sharing.

REQUIREMENTS and QUALIFICATIONS:

  • Fluency in English.
  • Minimum of two years’ project management experience in healthcare.
  • Strong team management and project management abilities.
  • Proficiency in clinical research methodologies and regulatory requirements.
  • Ability to manage complex schedules and budgets.
  • Independent and team-oriented work capabilities.
  • Ability to meet strict deadlines and handle stressful situations.
  • Effective delegation and escalation skills.

Required profile

Experience

Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Verbal Communication Skills
  • Adaptability
  • Analytical Thinking
  • Open Mindset
  • Leadership
  • Physical Flexibility

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