Join Clario Costa Rica as a Project Manager and support Cardiac Safety clinical trials. Our CS Project Manager is responsible for directing/managing services for client projects to assure high quality, on-time and on-budget services while promoting excellent customer service.

In this role you will:

• Lead the Planning and Setup, Monitoring, and Closeout phases of Cardiac Safety study management
• Monitor study timelines and manage the financial components of each study
• Identify potential study risks and mitigations, and escalate as appropriate.
• Manage internal/external negotiations and promote collaboration to foster a positive team environment, effective communications, and efficient use of resources to meet study timelines and contractual obligations.
• Apply problem solving strategies to address customer issues and maintain issue tracking documentation to monitor progress and ensure timely resolution to customer escalations
• Ensure compliance with timely training completion and documentation
• Present study services at Investigator Meetings or site initiation meetings as needed
• Attend client meetings with Business Development and/or Operational teams to present Company services and Operational Data flow, as needed
• Assist with training new members of the Project Management team and perform other duties, assignments, or special projects as time and/or circumstances necessitate.

The duties and responsibilities listed in this job description represent the major responsibilities of the position. Other duties and responsibilities may be assigned, as required. This job description and any attachments do not constitute or represent a contract.

What we seek:

• Bachelor Degree and/or proven demonstrated Project Management skills or experience within the industry
• 2-4+ years of experience in pharmaceutical field (or related industry experience), with an emphasis on project management. Prior clinical trial research and a good understanding of study protocol will be very helpful!
• Excellent organizational, interpersonal, time management, and prioritization skills
• Excellent verbal and written communication skills, including ability to communicate effectively in English
• Working knowledge of Microsoft Office products
• Knowledge of the pharmaceutical drug development process
• Detail oriented and demonstrated responsiveness to inquiries and requests
• Valid passport and ability to travel approximately 20%
• Ability to work from home on a regular basis (this role will be fully remote to start, although hybrid options will be

What we offer -

• Competitive Salary plus Annual bonus target
• Excellent On-Boarding plan
• Global Exchange Program
• Exceptional Tuition Reimbursement program
• Comprehensive Benefits Package

We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law. All are welcome - join us!

At Clario, we put people first, always. We are united and driven by patients, committed to making a difference, and we are always looking for the best talent to help us transform lives.