Program Manager at Clairo

Hanover, Lower-Saxony, Germany

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Not SpecifiedCompensation

Mid-level (3 to 4 years)Experience Level

Full TimeJob Type

UnknownVisa

Automotive, Battery, Energy StorageIndustries

Requirements

Bachelor Degree in Engineering or Business
Minimum 4 years work experience in Program Management in Automotive or equivalent
Proficient working experiences with project management methods (e.g. Auditing, PMI standards, IATF standards)
Proficient working experiences with PM related tools (e.g. Monday.com, Microsoft Office Applications, APQP, AIAG, Quality Systems)
Proficient working knowledge of production processes and areas, product designing and sales processes
PMP Certification or equivalent in certification or experience preferred
Demonstrated Customer and Supplier relationship management
Working knowledge of costing/quoting process
MS Project, MS Office, Outlook
Methodical knowledge in FMEA and SPC
Knowledge of manufacturing process specific to their products
Knowledge of design and development process
Strong communication skills
Fluency in English is a must, knowledge of German is a plus

Responsibilities

Execution and management of programs, according to budget and timing requirements
Lead Simultaneous Development Team (SDT) through Power D3 / ITP to launch program
Demonstrate proficiency in the use of program management related processes (e.g. ITP/PowerD3) as applicable
Understand customer needs, requirements and specifications. Leads team to insure prompt response to customer inquiries
Early identification of project risk and Initiation of mitigation plans
Precise, effective and clear communication to all levels of organization
Lead within a project (indirect leadership), enable and support others, personally engaged in coaching others for their development. Motivate to encourage excellence
Planning & conduction of Program Reviews
Ensure timeliness gate exits
Solve conflicts and escalation in a good way by involving all parties
Make decisions and achieve results that are consistent with company and team values. Support and drive in building a strong team structure

Skills

Program Management

Project Management

PMI Standards

IATF Standards

Auditing

PowerD3

ITP

Risk Management

Cross-functional Leadership

Automotive

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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