RQM+ is The MedTech CRO, accelerating innovation to patient impact. Our tailored solutions deliver regulatory and quality expertise, FDA-recognized laboratory services, clinical trials, and reimbursement strategies across device types and therapeutic areas to bring life-changing technologies to patients — faster, safer, better.
We don’t make MedTech. We make MedTech happen.
Our experienced teams are cohesive, collaborative, and proactive, constantly seeking to improve and evolve while remaining laser-focused on customer success. RQM+ elevates the MedTech experience through best-in-class service and clear, concise communication. We serve as an extension of our customers establishing and maintaining excellent client and site relationships and providing direct access to our technology platforms for real-time data and study transparency.
Job Summary:
The Clinical Research Associate (CRA) participates in the preparation and execution of pre-market to post-market clinical investigations. Oversees the progress of clinical investigations by conducting site qualification, initiation, interim monitoring and close out visits to clinical sites. Monitors clinical investigations in accordance with Good Clinical Practice/ISO 14155 and procedures set forth by RQM+ and sponsors. Works closely with the Project Manager and/or Lead CRA to ensure all monitoring activities are conducted according to study requirements.
Primary Responsibilities:
Performs site initiation activities, reviewing with the site personnel the clinical investigation plan, regulatory status, study procedures, and provides training on completion of the eCRF, monitoring activities and study close-out activities.
May review clinical investigation plans, eCRFs, study manuals and other related documents, as requested by the Project Manager and/or Lead CRA.
Serves as primary contact between RQM+, sponsor and investigator; coordinates all correspondence; ensures timely transmission of clinical data with the study site and technical reporting, as requested.
Performs study close-out visits per the study specific Clinical Monitoring Plan including final study product reconciliation and disposition, site study file reconciliation, data query resolution through to database lock and resolution of outstanding action items.
Assists with, and attends, Investigator Meetings for assigned studies.
Authorized to request site audits due to data integrity concerns and the preparation of the monitoring manual
Attends study-related, company, departmental, and external meetings, as required.
Ensures internal and study-related trainings are completed per RQM+ process and/or study timelines, including updating the study level study management system.
Ensures all study deliverables are completed per RQM+ and study timelines.
Serves as mentor for junior staff and those new to the company and/or study.
Performs other duties, as requested.
Education/Work Experience/Requirements:
University / College degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing, certification, medical or laboratory technology), or equivalent combination of education and experience.
Knowledge of medical terminology, clinical research acronyms and medical / scientific abbreviations.
Ability to perform clinical data review of source documents and case report forms independently and accurately
Able to follow study specific guidelines, plans, manuals and participate in all aspects of training in addition to performing verification and resolution of data queries / discrepancies within defined timelines
Understanding and following oral and written instructions precisely
Solid communication skills with co-workers, investigative site and sponsor / vendor required
Working in a fast-paced environment and adapt easily to changing priorities
Located in Germany with excellent German language skills, good knowledge in English (writing, reading, speaking) and preferably in French (writing, reading, speaking)
Ability to read and interpret study protocols, investigator brochures, study manuals and ancillary documents such as SOPs and equipment and laboratory procedure manuals
Process the ability to write routine reports and correspondence, to speak effectively before groups of customers or at sites
Applying common sense understanding to carry out instructions furnished in written, oral or diagram form
Process the ability to deal with problems involving several concrete variables in standardized situations
Good knowledge in the current Microsoft Office Suite
Customer Focus: Is dedicated to meeting the expectations and requirements of internal and external customers; gets first-hand customer information and uses it for improvements in product and services
Acting with customers in mind, establishing and maintaining effective relationships with customers and gains their trust and respect
Ability to travel (approx. 40-70%)
Behaviors: Action-Oriented, Approachability, Building Effective Teams, Business Acumen, Career Ambition, Composure, Courage (Managerial), Customer Focus, Decision Quality, Informing, Integrity & Trust, Interpersonal Savvy, Planning
Supervisory Responsibilities: This position does not have supervisory responsibilities.
Salary: €53,355.18 - €66,693.72
Work Environment/Equal Opportunity
This job operates in a professional office environment in a global organization. This role routinely uses standard office equipment such as computers, phones, photocopiers, and filing cabinets. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. The employee is occasionally required to sit; climb or balance; and stoop, kneel, crouch, or crawl.
We are committed to promoting equality of opportunity for all staff and job applicants. We aim to create a working environment in which all individuals can make best use of their skills, free from discrimination or harassment, and in which all decisions are based on merit.
Our selection for recruitment does not discriminate based on age, disability, gender reassignment, marital or civil partner status, pregnancy or maternity, race, color, nationality, ethnicity, ethnic or national origin, religion or belief, sex or sexual orientation or gender reassignment status (protected characteristics).
Being an industry leader in Medtech is just the beginning for RQM+. We consider our employees our biggest asset and we invest heavily in ongoing learning and development. Providing a rewarding place to work is rooted deep in our core values. From an industry leading compensation package to a deeply engrained focus on work life balance, RQM+ has a unique offering for regulatory and quality professionals. At RQM+, you are not just another employee, you are a member of RQM+ family. Make your impact today!
We invite you to apply if you have an interest in learning more about our organization and beginning your journey with us.
Job Opportunity Verification
At RQM+, we prioritize the security of our job applicants. To ensure a safe application process:
All legitimate RQM+ job opportunities are listed on our official careers page: rqmplus.com/careers
Every candidate going through the interview process will participate in a voice and/or video interview.
Exercise caution with unsolicited job offers or requests for sensitive information.
