Full-Time

Lead Project Manager

Ecoa

Posted on 11/6/2024

Clairo

Clairo

5,001-10,000 employees

Generates clinical evidence for trials

Biotechnology
Healthcare

Senior

Remote in USA

Category
Project Management
Business & Strategy
Requirements
  • Bachelor’s degree and proven Project Management skills or experience within the industry, including expertise in primary service line and/or support of studies in multiple service lines.
  • Demonstrated ability to mentor staff.
  • 5-10 years of experience in pharmaceutical field (or related industry experience), with an emphasis on project management.
  • Knowledge of the drug development process.
  • Ideally experience within eCOA or similar industry products.
  • Software Development Life Cycle (SDLC) experience.
  • 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%.
Responsibilities
  • Manage designated Project Management staff, which includes:
  • Mentoring and defining career paths by developing core competencies.
  • Ensuring proper training is executed and documented.
  • Conducting reviews of system set-ups and documents to ensure high quality of deliverables in accordance with quality standards and SOPs.
  • Coordinating routine status meetings to facilitate communications, monitor workload, and provide forecasting guidance.
  • Collecting and monitoring defined staff metrics.
  • Independently lead the Planning and Setup, Monitoring, and Closeout phases of program/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.
  • 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.
  • Provide primary service line support to cross-trained team members from other service lines
  • May serve as point of contact for focus areas within service lines
  • Influence strategic decision making and implement departmental objectives according to schedule
  • Serve as department lead for operational readiness regarding new product initiatives as applicable within Line of Business
  • May guide study teams in being consistent across Therapeutic Area or Program as pertinent to ensure customer is consistent in study set up, optimizing efficiencies and following customer program objectives
  • 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 and participate in sales initiatives to generate incremental revenue
  • Assist with developing training plans and training new members of the Project Management team
  • Perform other duties, assignments, or special projects as time and/or circumstances necessitate

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, allowing for flexibility in how studies are conducted. Clario's extensive experience, with nearly 50 years in the field, 19,000 clinical trials, and 870 regulatory approvals, enables them to provide reliable and rich data to their partners. Unlike many competitors, Clario's global presence with 30 facilities across nine countries enhances their ability to conduct trials at scale. The company's goal is to empower partners in the healthcare industry to improve patient outcomes through high-quality clinical evidence.

Company Stage

Growth Equity (Venture Capital)

Total Funding

$29.9M

Headquarters

London, United Kingdom

Founded

1972

Growth & Insights
Headcount

6 month growth

0%

1 year growth

0%

2 year growth

0%
Simplify Jobs

Simplify's Take

What believers are saying

  • 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.

What critics are saying

  • 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.

What makes Clairo unique

  • 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.

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Benefits

Competitive and equitable total rewards package

Physical, mental and financial health and wellness

Flexible working approach

INACTIVE