Clairo

Project Manager, eCOA

Costa Rica

Not SpecifiedCompensation
Junior (1 to 2 years)Experience Level
Full TimeJob Type
UnknownVisa
PharmaceuticalsIndustries

Position Overview

  • Location Type:
  • Job Type: Full time
  • Salary:

Responsible for directing and managing services for client projects to assure high quality, on-time, and on-budget services while promoting excellent customer service.

Essential Duties and Responsibilities

  • Lead the Planning and Setup, Monitoring, and Closeout phases of study management, which includes:
    • Gathering customer requirements and relaying to internal teams
    • Developing study documentation
    • Distributing/tracking equipment
    • Creating/distributing reports
    • Archiving study data and documentation
    • Appropriate setting and fulfilling of customer expectations
  • Monitor study timelines and manage the financial components of each program/study, which includes:
    • Budget reviews
    • Revenue forecasting
    • Scope changes
    • Invoice reconciliation
  • 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.

Other Duties and Responsibilities

  • Ensure compliance with timely training completion/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.
  • Perform other duties, assignments, or special projects as time and/or circumstances necessitate.

Qualifications and Skills Needed

  • Education: Bachelor’s degree and/or proven Project Management skills or experience within the industry.
  • Experience: 1-4 years of experience in project management with an emphasis in the pharmaceutical field (or related industry experience). Ideally experience within eCOA or similar industry products.
  • Software Development Life Cycle (SDLC) experience.
  • Knowledge of the drug development process.
  • 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.
  • Detail-oriented and demonstrated responsiveness to inquiries and requests.
  • Valid passport and ability to travel approximately 20%.

Company Information

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.

Additional Notes

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. Clario reserves the right to amend or change this job description to meet the needs of Clario. This job description and any attachments do not constitute or represent a contract. The Department Head has the discretion to hire personnel with a combination of experience and education, which may vary from the above listed qualifications.

Skills

Project Management
Study Planning
Study Monitoring
Study Closeout
Customer Requirements Gathering
Study Documentation
Report Distribution
Data Archiving
Budget Management
Revenue Forecasting
Scope Management
Invoice Reconciliation
Risk Management
Negotiation
Collaboration
Problem Solving
Issue Tracking
Training
Presentation

Clairo

Generates clinical evidence for trials

About Clairo

Clario specializes in generating clinical evidence for medical research by utilizing a comprehensive technology platform. Their services support various types of clinical trials, including decentralized, hybrid, and site-based trials. Clario's approach combines nearly 50 years of experience with a vast network of facilities across nine countries, allowing them to conduct a significant number of clinical trials and regulatory approvals. What sets Clario apart from competitors is their extensive expertise and the ability to provide a wide range of endpoint technologies, which enhances the quality of evidence produced. The company's goal is to empower partners in the healthcare industry to improve patient outcomes through reliable and rich clinical data.

London, United KingdomHeadquarters
1972Year Founded
$29.9MTotal Funding
GROWTH_EQUITY_VCCompany Stage
Biotechnology, HealthcareIndustries
5,001-10,000Employees

Benefits

Competitive and equitable total rewards package
Physical, mental and financial health and wellness
Flexible working approach

Risks

Increased competition from AI-driven platforms like Medable may threaten Clario's market share.
The IPO filing may lead to investor pressure for rapid financial returns, affecting strategy.
AI integration from ArtiQ poses data privacy and compliance risks, especially in the EU.

Differentiation

Clario offers a comprehensive endpoint technology platform for diverse clinical trial models.
The company has nearly 50 years of experience in clinical trial technology solutions.
Clario's global presence includes 30 facilities across North America, Europe, and Asia Pacific.

Upsides

Clario's IPO aims for a valuation of over $10 billion, indicating strong market confidence.
The FDA clearance of SpiroSphere® with wireless ECG enhances Clario's clinical trial capabilities.
Clario's acquisition of ArtiQ boosts its AI capabilities in respiratory clinical trials.

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