Project Manager

Costa Rica

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Not SpecifiedCompensation

Mid-level (3 to 4 years), Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

Project Management ServicesIndustries

Requirements

Candidates should possess a Bachelor's degree and/or proven project management skills or industry experience, with 1-4 years of experience in project management, preferably in the pharmaceutical field. A working knowledge of Microsoft Office products and excellent organizational, interpersonal, time management, prioritization, verbal, and written communication skills are essential. Knowledge of the drug development process and detail orientation are also required, along with the Clario PM Certification as applicable.

Responsibilities

The Project Manager will direct and manage client projects, ensuring high quality, on-time, and on-budget delivery while promoting excellent customer service. Responsibilities include leading the planning, monitoring, and closeout phases of study management, gathering customer requirements, developing study documentation, distributing and tracking equipment, creating reports, and archiving study data. The role involves monitoring study timelines, managing financial components like budget reviews and revenue forecasting, identifying and mitigating study risks, managing negotiations, and resolving customer issues. Additional duties include ensuring timely training completion, presenting study services at meetings, attending client meetings, assisting with training new team members, and performing other assigned duties.

Skills

Project Management

Client Relationship Management

Budget Management

Scope Management

Risk Management

Negotiation

Problem Solving

Customer Service

Data Archiving

Reporting

Training

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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