Clairo

Program Manager (Cardiac and Respiratory) (f/m/d)

United States

Not SpecifiedCompensation
Senior (5 to 8 years), Expert & Leadership (9+ years)Experience Level
Full TimeJob Type
UnknownVisa
Healthcare, Medical DevicesIndustries

Program Manager (Cardiac and Respiratory) (f/m/d)

Employment Type: Full-time

Position Overview

Enhance your career as a Program Manager (Cardiac and Respiratory) (f/m/d). This role is responsible for maintaining specific client relationships and standards by providing client-specific support and direction to the Project Management team for relevant projects. The goal is to ensure high-quality, on-time, and on-budget services while promoting excellent customer service. We are looking for talents in the UK, Germany, or Hungary who can make a difference every day by sharing their knowledge with peers and fostering a culture of great communication and client support.

What We Offer

  • Competitive compensation
  • Attractive benefits (security, flexibility, support, and well-being)
  • Engaging employee programs

Responsibilities

  • Ensure consistency of delivery across programs of work by setting up standards, sharing lessons learned, and communicating client/program-specific requirements to internal teams allocated to the programs.
  • Serve as a member of Oversight/Operations Committees for any assigned clients.
  • Organize or contribute to partnerships with assigned clients and Clario internal teams to proactively review and discuss study risks, mitigation plans, statuses, opportunities, improved delivery, increased profitability, quality, and client satisfaction.
  • Ensure Clario is addressing any project or program issues for assigned clients and effectively driving resolution in a timely manner.
  • Monitor study timelines and manage the financial components across the portfolio of projects on assigned accounts.
  • 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.
  • Develop and apply problem-solving strategies to address customer issues and maintain issue-tracking documentation to monitor progress and ensure timely resolution to customer escalations.
  • Monitor and report Program level KPIs on an as-needed basis (e.g., monthly or quarterly).
  • Attend operational meetings and governance meetings with customers (in-person and remote).
  • Provide primary service line support to cross-trained team members from other service lines.
  • Influence strategic decision-making and implement departmental objectives according to schedule.
  • Ensure compliance with timely training completion/documentation.
  • Present study services at Investigator Meetings, Site Initiation meetings, Vendor Kick-off meetings, or other sponsor/study-related meetings as needed.
  • Attend client meetings with Business Development and/or Operational teams to present Company services and Operational Data flow, as needed, and participate in sales initiatives to generate incremental revenue.
  • Assist with developing training plans and training new members of the Project Management team onto assigned accounts.
  • Perform other duties, assignments, or special projects as time and/or circumstances necessitate.

Requirements

  • Bachelor’s Degree and proven Project Management skills or experience within the industry, including expertise in the primary service line and/or support of studies in multiple service lines.
  • 1.5 years of experience as a manager.
  • 4-8 years of experience in the pharmaceutical field (or related industry experience), with an emphasis on project management.
  • Knowledge of the drug development process.
  • Excellent organizational, interpersonal, time management, and prioritization skills.
  • Excellent verbal and written communication skills, including the ability to communicate effectively in English.
  • Working knowledge of Microsoft Office products.
  • Detail-oriented and demonstrated responsiveness to inquiries and requests.

Company Information

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. We value the contribution each of our people brings. It’s only through our people that we can continue to...

Skills

Program Management
Client Relationship Management
Project Management
Quality Assurance
Budget Management
Customer Service
Risk Management
Negotiation
Problem Solving
Team Collaboration
Communication

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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