Data Manager I at Clairo

Shanghai, Shanghai, China

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Not SpecifiedCompensation

Junior (1 to 2 years), Mid-level (3 to 4 years)Experience Level

Full TimeJob Type

UnknownVisa

Clinical Research, Healthcare, PharmaceuticalIndustries

Requirements

BS/BA Degree in Life Sciences or related field preferred
Minimum of 2 years Data Management or related experience preferably

Responsibilities

Serve as the primary internal and Sponsor contact for Data Management questions, issues, or concerns including data collection, data cleaning, data delivery, data reconciliation, database lock, and Data Management activity timelines
Define the Data Management Plan (DMP) by collaborating with Sponsors to define study requirements, determining standard edit checks and defining new ones as needed, documenting data processing guidelines, collaborating on study setup requirements, communicating DMP contents to internal CDM teams, and completing data management related information within internal systems
Lead the development, review, and finalization of data transfer requirements, including providing or customizing ERT standard file specifications, reviewing Sponsor-defined specifications, coordinating finalization and approval, maintaining approved specifications, performing validation of file formats or data content, submitting SAS programming requests, generating sample data, providing sample data and Sample Data Approval Form to Sponsors, maintaining signed forms, and managing database lock activities and timelines
Serve as the primary point of contact for DCRs and query escalation, addressing sponsor or site concerns by working with data coordinators and project managers
Ensure good quality of study set-ups by participating in the review and/or approval process for Data Management components
Ensure high customer satisfaction by delivering on promises, meeting timelines, and providing excellent customer service
Identify out of scope requests and elevate them to the Project Manager for billing through the Change Order process
Ensure Data Management Files are up-to-date and comprehensive, including Data Management Plans, File Specifications, Data Transfer Agreements, Data Correction Forms and Requests, client emails, etc
Conduct routine status meetings with Sponsor/CRO and internal teams, providing agenda and meeting minutes to all attendees
Process at least one routine data run per assigned study per quarter and perform all sample, complete, and final data sends
Assist in the preparation of monthly reporting by providing metrics as required
Communicate project status clearly with Sponsors, Project Management, and internal Client specific teams

Skills

Data Management

Data Cleaning

Data Reconciliation

Edit Checks

Data Transfer Specifications

SAS Programming

Database Lock

Data Management Plan

Data Collection

Data Processing

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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