Clinical Data Spec

Medtronic; United States; Remote; USD 40,000 - 60,000; Full time

Benefits offered by this job

Medtronic Incentive Plan (MIP)

Job summary

Medtronic in the United States seeks a Clinical Safety Specialist to drive data-driven safety at the clinical level, collaborating across teams to collect and review clinical data.

You will design protocols, organize data systems, resolve discrepancies, and prepare reports for regulatory validation, contributing to safer, innovative therapies that change lives.

This role emphasizes practical knowledge, advanced education, and the ability to work independently within the specialist career stream.

Qualifications

• Requires practical knowledge in clinical data collection and safety.
• Bachelor's degree or higher; advanced degree with 0 years of experience acceptable.
• Experience in data review and regulatory reporting is desirable.

Responsibilities

• Collaborates with stakeholders on the design, data collection, testing and implementation of clinical data studies.
• Designs and implements clinical protocols and data collection systems.
• Develops systems for organizing data to analyze, code, identify and report trends.
• Reviews data discrepancies and ensures cross-project consistency.

Skills

Clinical data collection

Data management

Protocol design

Regulatory reporting

Cross-functional collaboration

Education

Bachelor's degree or higher

Job description

Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.

A Day in the Life

Business title will be Clinical Safety Specialist.

Responsibilities may include the following and other duties may be assigned.

• Collaborates with variousstakeholderson the design, documentation, testing and implementation of clinical data collection studies, and clinical data review.
• Design and implement clinical protocols and data collection systems.
• Develops systems for organizing data to analyze, code,identify and report data and trends.
• Manages data management issues by reviewing protocols for cross-project consistency and identifying standard Case Report Form (CRF) modules to meet objectives.
• Provide early strategic input on protocol design focused on safety and/or data management issues.
• Review and resolve data discrepancies for standardized data validation systems and procedures.
• Prepares reports of clinical trial studies for internal validation and cross validation studies.
• Reports out in compliance with Regulatory reporting requirements.

SPECIALIST CAREER STREAM: Typically an individual contributor with responsibility in a professional discipline or specialty. Delivers and/or manages projects assigned and works with other stakeholders to achieve desired results. May act as a mentor to colleagues or may direct the work of other lower level professionals. The majority of time is spent delivering and overseeing the projects – from design to implementation - while and adhering to policies, using specialized knowledge and skills normally acquired through advanced education.

DIFFERENTIATING FACTORS

Autonomy: Established and productive individual contributor.
Works independently with general supervision on larger, moderately complex projects / assignments.

Organizational Impact: Sets objectives for own job area to meet the objectives of projects and assignments.
Contributes to the completion of project milestones .
May have some involvement in cross functional assignments.

Innovation and Complexity: Problems and issues faced are general, and may require understanding of broader set of issues or other job areas but typically are not complex .
Makes adjustments or recommends enhancements in systems and processes to solve problems or improve effectiveness of job area.

Communication and Influence: Communicates primarily and frequently with internal contacts.
External interactions are less complex or problem solving in nature.
Contacts others to share information, status, needs and issues in order to inform, gain input, and support decision-making.

Leadership and Talent Management: May provide guidance and assistance to entry level professionals and / or employee in Support Career Stream.

Required Knowledge and Experience: Requires practical knowledge and demonstrated competence within job area typically obtained through advanced education combined with experience.
Requires a Baccalaureate degree (or for degrees earned outside of the United States, a degree which satisfies the requirements of 8 C.F.R. § 214.2(h)( 4)(iii)(A) and minimum of 2 years of relevant experience, or advanced degree with 0 years of experience.

Physical Job Requirements

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.

Benefits & Compensation

Medtronic offers a competitive Salary and flexible Benefits Package
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.

Pay range / Rango salarial / Intervalo salarial /Fascia retributiva / Tranche de salaire / Gehaltsband / Salaribereik: Italy: 40,000.00 EUR- 60,000.00 EUR|

The final salary within this range will be determined based on objective, job-related criteria, including relevant experience, skills and qualifications, in accordance with our compensation framework.

This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).