Clairo

Assistant Clinical Project Manager

Costa Rica

Not SpecifiedCompensation
Junior (1 to 2 years)Experience Level
Full TimeJob Type
UnknownVisa
Pharmaceuticals, Clinical ResearchIndustries

Position Overview

  • Location Type: Not specified
  • Employment Type: Full Time
  • Salary: Not specified
  • Brief Description: This role assists Clinical Project Managers with project administration and support, contributing to the successful execution of clinical trials. Responsibilities include drafting documents, reviewing presentations, participating in meetings, and serving as a liaison with cross-functional teams. The position also involves monitoring data flow, responding to inquiries, and ensuring adherence to project timelines and quality standards.

Requirements

  • Education: Bachelor’s Degree preferred
  • Experience: 0-1 year experience working with clinical trials and/or within a pharmaceutical environment preferred.
  • Skills:
    • Ability to work in a group setting and independently.
    • Ability to adjust to changing priorities.
    • Excellent attention to detail and orientation towards meticulous work.
    • Strong interpersonal and communication skills (both verbal and written).
    • Strong organizational skills.
    • Goal-oriented.
    • Ability to project and maintain a professional and positive attitude.
    • Familiarity with Microsoft Office Programs preferred.

Responsibilities

Primary Responsibilities:

  • Drafting project documents.
  • Reviewing and editing project presentations.
  • Participating in project meetings, conference calls, and training calls.
  • Reading and understanding project protocol documents.
  • Acting as a liaison with cross-functional team members to ensure timely completion of all study deliverables.
  • Reporting study needs and issues.
  • Assisting Clinical Project Managers in maintaining, reviewing, and communicating project progress.
  • Monitoring internal data flow to ensure completion of tasks within agreed-upon timeframes.
  • Responding to inquiries in a professional, courteous, and timely manner.
  • Communicating with clients regarding project status.
  • Verifying protocol imaging requirements are met and queries appropriately identified.
  • Serving as acting Project Manager in the absence of the assigned Project Manager.
  • Mentoring, guiding, and supporting the Operations team, including providing feedback to the Operations Manager for performance appraisals.
  • Ensuring the development and adherence to project timelines as they relate to therapeutic processes.
  • Assisting in tracking and resolving client issues.
  • Serving as an additional point of contact to clients, sites, sponsors, etc.
  • Keeping supervisor advised of current issues.

Secondary Responsibilities:

  • Contributing to team effort by helping others achieve results.
  • Performing other duties as assigned.
  • Maintaining technical knowledge by attending and participating in applicable company-sponsored training.

Working Conditions

  • Travel: 0-5%
  • Lifting: 0-15 lbs
  • Other: Computer work for long periods of time

Company Information

  • EEO Statement: Clario is an equal opportunity employer. Clari evaluates qualified applicants without regard to race, color, religion, gender, nation.

Skills

Project Documentation
Presentation Review
Meeting Participation
Protocol Understanding
Cross-functional Communication
Data Monitoring
Client Communication
Microsoft Office

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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