Candidates

Specialization &
Roles We Outsource

At ACR, our commitment to advancing the MedTech industry is reflected in the specialized roles we provide to our clients. Our comprehensive understanding of the sector’s needs allows us to offer a diverse pool of talent, ensuring that we can fill any niche or gap within your organization. Here are some of the specialized roles we focus on outsourcing:

Clinical Research Associates (CRAs)

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Biostatisticians

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Clinical Data
Managers

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Clinical Project Managers

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Medical
Writers

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Regulatory Affairs Specialists

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Quality Assurance (QA) Professionals

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ACR enables MedTech companies to fill critical positions with qualified individuals who possess the specific skills and experience needed to meet the industry’s challenging demands. Our focus on specialized talent ensures that we provide not just staff, but true professionals capable of contributing to the success and innovation of the MedTech industry.

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Calle Fernando el Santo 27

28010 Madrid, Spain

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+ 34 914 320 709
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Clinical Research Associates (CRAs)

Our CRAs are the backbone of clinical trial monitoring, ensuring compliance with study protocols, standard operating procedures, and regulatory requirements. They are adept at site management, patient enrollment, and data integrity, providing crucial oversight throughout the clinical trial process.

Biostatisticians

Our Biostatisticians provide expertise in statistical programming, data analysis, and interpretation. They are crucial in the design of clinical trials, the development of statistical analysis plans, and the interpretation of study results, ensuring data-driven decision-making throughout the product lifecycle.

Clinical Data Managers

Clinical Data Managers are key in managing the collection, integration, and availability of data critical for clinical research. They ensure the accuracy and consistency of clinical trial data, facilitating its analysis and reporting.

Clinical Project Managers

Project Managers specialized in the MedTech clinical investigations are experts at driving project completion on time and within budget. They coordinate cross-functional teams, manage resources, and maintain clear communication channels to ensure the successful execution of projects.

Medical Writers

Medical Writers craft clear and compliant documentation essential for regulatory submissions, clinical trial reporting, and publication. Their skills are vital for conveying complex information in a precise and accessible manner, bridging the gap between scientific data and its stakeholders.

Regulatory Affairs Specialists

Regulatory Affairs Specialists are essential in navigating the complex regulatory landscape, assisting with submission strategies, regulatory documentation, and communications with regulatory agencies. Their expertise ensures that products meet all regulatory standards, facilitating successful market entries and compliance.

Quality Assurance (QA) Professionals

QA Professionals play a critical role in maintaining the quality and safety of medical devices. They are instrumental in implementing and overseeing quality management systems, conducting audits, and ensuring adherence to industry standards and regulatory guidelines.