Clairo

Sr. Clinical Data Manager

Costa Rica

Auto‑apply with AI Apply

Not SpecifiedCompensation

Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

Clinical Trials, Pharmaceuticals, HealthcareIndustries

Requirements

Candidates should possess a Bachelor’s degree in a related scientific field, such as biology, chemistry, or a related discipline, and have a minimum of 7 years of experience in clinical data management. Strong knowledge of clinical trial data management principles, data standards (e.g., CDISC), and regulatory requirements (e.g., GCP, FDA) is essential, along with experience working with clinical trial databases and electronic data capture (EDC) systems.

Responsibilities

The Sr. Clinical Data Manager will ensure clinical trial databases meet project requirements by creating and updating study data management documentation, collaborating with project teams, and participating in study team meetings. They will also work with senior staff to execute data management deliverables, understand study requirements, perform study setup, coordinate data receipt, and develop study-specific procedures. Furthermore, the role involves attending Kick-Off Meetings, participating in sponsor meetings, reviewing documentation, and developing timelines to ensure CDM project milestones are met in coordination with the project team.

Skills

Data management

Study documentation

Study oversight

Escalation management

Study coordination

Project collaboration

Study documentation review

Study-specific edit check development

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.

Key Metrics

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.

Land your dream remote job 3x faster with AI

Try Jobo Free