The Clinical Affairs Scientist will provide guidance to study sponsors and IVD medical device manufacturers in support of clinical study design and execution. Responsible for the development of clinical study protocols and implementation of those protocols at study sites, the Clinical Affairs Scientist develops and implements strategies in a collaborative environment between colleagues and clients with the goal of successful regulatory submissions.

About MDC Associates

For over 30 years, MDC has helped innovators and entrepreneurs bring in vitro diagnostics (IVD) and medical devices to market and impact the lives of millions of patients around the world. Our mission is to continue to support these innovators by applying our expertise in Regulatory Affairs, Quality Systems, Training, and other consulting services to help them launch new advances that promote and protect our global and local communities’ health. Learn more at www.mdcassoc.com.

By joining MDC, you will experience opportunities to grow your skillset and advance your career in a culture where we value everyone, and where we know our success is directly tied to yours. Take the next step to explore an opportunity with MDC by applying for this position.

MDC Associates, Inc. is an Equal Opportunity Employer committed to a diverse workforce. MDC Associates, Inc. will not discriminate against any worker or job applicant based on race, color, religion, gender, gender identity, national origin, ancestry, age, sexual orientation, gender identity, marital or civil partnership status, gender reassignment, non-job related mental or physical disability, genetic information, veteran status, military service, or membership in any other category protected under law.

Responsibilities

• Development of clinical study strategies and protocols to support the validation of new medical and in vitro diagnostic devices
• Prepare and present clinical study strategies and protocols for regulatory bodies including the US FDA
• Creation of Clinical and Analytical Study Protocols and supporting plans and procedures, including Informed Consent Forms (ICFs), Monitoring Plans and Data Collection Forms in conjunction with the assigned Project Team
• Assist clients in identifying and contracting with potential Clinical Trial Sites and/or Reference Laboratories
• Assist with Institutional Review Board (IRB) submissions
• Lead and Manage internal and external resources to support all aspects of clinical and method comparison studies in accordance with Good Clinical Practice
• Monitor and analyze clinical study data and report on performance both internally and with study sponsors
• Prepare study reports to support Regulatory Filings such as FDA 510(k), de novo and PMA submissions, Health Canada Licensure, EU Technical Files, etc
• Provide input on content of submission documents based on experience, regulations and guidance available from regulatory bodies
• Implementation of regulatory and clinical processes as they relate to company procedures, clinical studies, testing, and documentation and ensure that they are communicated through company policies and procedures

Qualifications

• Bachelor’s degree in a health care or other scientific discipline or educational equivalent
• Five to Ten years of experience in a clinical environment or medical devices industry, with specific experience in in vitro diagnostic devices
• In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP), International Conference on Harmonisation (ICH), and HIPAA guidelines
• Understanding of U.S. Food and Drug Administration (FDA) laws and guidance
• Understanding of IRB guidelines and Common Rule
• Knowledge of the European Commission Medical and In Vitro Diagnostic Device Regulations
• Knowledge of applicable protocol requirements as provided in company training
• Computer skills including proficiency in use of Office 365, Microsoft Word, Excel, Access, Outlook and PowerPoint
• Strong written and verbal communication skills including good command of English language
• Excellent organizational and problem-solving skills
• Effective time management skills, attention to detail, and accuracy in work
• Ability to manage competing priorities without compromising quality
• Ability to establish and maintain effective collaborative relationships with coworkers, managers and clients

Travel Requirements

Approximately 25% domestic travel expected, with the potential for international locations.

Travel may include attending off-site client meetings, attending clinical site Initiation and Monitoring Visits, as well as attending annual industry conferences (i.e.: Clinical Virology Symposium, American Association for Clinical Chemistry, American Society for Microbiology)

Reports To

Senior Clinical Affairs Scientist

Location

Beverly, Massachusetts OR Remote

Our offices are within easy walking distance from the Beverly Depot, allowing for a green commute from Boston and the NorthShore (both Newburyport and Rockport lines).

Pay and Benefits

MDC Associates, Inc, offers competitive salaries and benefits, including health/dental, HRA, and 401k with a match. We also support an engaging work environment that provides everyone the opportunity and structure to learn and grow.