Associate Data Manager at Clairo

Budapest, Hungary

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Not SpecifiedCompensation

Junior (1 to 2 years)Experience Level

Full TimeJob Type

UnknownVisa

Clinical Research, HealthcareIndustries

Requirements

BS/BA Degree in Life Sciences or related field
Minimum of 2 years experience working with clinical research/data
Familiarity with clinical data reports, GCP, and general understanding of clinical trials
Strong organizational, interpersonal, analytical and communication skills
Detail-oriented
Experience with Windows and Microsoft Office products preferred
Ability to communicate effectively in English
SAS and/or SQL exposure or experience a plus
Knowledge of CDISC SDTM is a plus

Responsibilities

Perform quality and/or consistency checks on the output file(s) generated by study specific programs where required, including comparing individual data points of the final output data to the corresponding data points of the original dataset based upon the gathered requirements and/or edit check output
Communicate with appropriate Clario staff (i.e. Data Manager, Science teams, medical staff) regarding any discrepancies found and document all results and/or changes
Work on study documentation (DMP/DTS) under the guidance of the Data Manager and assist in getting study documentation prepared for client review
Serve as a point of contact for updates needed to the CDM task schedule (i.e. edit checks, transfer scheduling, Final data transfer checklist, etc.) and ensure they are being completed and/or maintained
Assist with metrics related to data issues or file delivery as well as ensuring the systems have correct information regarding study assignment
Provide assistance to CDM team for documents, presentations, etc. that require template updates and formatting changes
Serve as primary recipient of client reconciliation feedback between data transfers and ensure appropriate investigation and/or action on those requests within the agreed turnaround time
Ensure good quality documentation is maintained in regard to the client reconciliation feedback
Communicate project status clearly with Clients and Project Management
Assist with the maintenance and storage of study documentation relative to data management activities
Contribute to continuous process improvement including workflow efficiencies and associated workflow documentation
Assist in CAPA issues related to study-specific data management activities

Skills

Key technologies and capabilities for this role

Data ManagementQuality ChecksData ReconciliationEdit ChecksData TransferCDMDMPDTSMetrics TrackingStudy Documentation

Questions & Answers

Common questions about this position

What compensation and benefits does Clario offer?

Clario offers competitive compensation and attractive benefits including security, flexibility, support, well-being, engaging employee programs, a flexible hybrid working model, and OTP Szép Card.

Is this role remote or office-based?

The role is located in the Budapest office with a flexible hybrid working model.

What skills and qualifications are required for the Associate Data Manager role?

Requirements include a BS/BA Degree in Life Sciences or related field, minimum of 2 years experience working with clinical research/data, familiarity with clinical data reports, GCP, and clinical trials, strong organizational, interpersonal, analytical and communication skills, and detail-oriented.

What is the company culture like at Clario?

Clario puts people first, is united and dynamic, values collaboration with internal and external teams, data integrity, and continuous process improvement.

What makes a strong candidate for this position?

A strong candidate has a degree in Life Sciences, 2+ years in clinical research/data, strong organizational and communication skills, detail-orientation, and pluses like SAS/SQL experience, CDISC SDTM knowledge, and Microsoft Office proficiency.

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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