Field Senior Clinical Research Associate

North American Science Associates, Inc.; Northern (KY); Remote; USD 69,000 - 134,000; Full time

Job summary

North American Science Associates, Inc. (NAMSA) is seeking a Senior Clinical Research Associate for remote USA work. The role focuses on maintaining human subject protection, GCP, and regulatory compliance while coordinating site monitoring across studies.

The candidate should have a higher education degree and 5+ years in clinical trials, with 3+ years in monitoring and 1 year device trial experience. SoCRA/ACRP certification is a plus. Travel up to 80% may be required.

Qualifications

• Fluency in English and local language, if different, required.
• Higher education degree or equivalent education, training, and experience.
• Preferred 5 years clinical trial experience.
• Preferred 3 years monitoring experience.
• Preferred 1 year device trial experience.
• Certifications such as SoCRA or ACRP preferred but not required.

Responsibilities

• Works on assigned studies to ensure human subject protection, GCP, and regulations.
• Coordinates and manages clinical site monitoring for assigned studies.
• May conduct on-site and remote monitoring visits.
• Serve as primary point of contact for site questions.
• Communicates site performance, trends, and concerns to study team.
• Supports study start-up activities and quality review of documents.
• Performs study-related training and maintains study documents.
• Tracks site and study metrics including enrollment and deviations.
• Participates in meetings with prospective clients and mentors CRAs.

Skills

Fluency in English

Higher education degree

5 years clinical trial experience

3 years monitoring experience

1 year device trial experience

Certification (SoCRA/ACRP) preferred

Education

Bachelor's degree or equivalent

Job description

## Field Senior Clinical Research AssociateApply: Remote - USA: Full time: Posted 30+ Days Ago: R5385NAMSA pioneered the industry and was the first independent company in the world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976.We are shaping the industry. NAMSA has been a key contributor to the development of the test methods that govern our industry. We have become the industry’s premier provider. We provide support for clients during every step of the product development lifecycle and beyond.Come and work for an organization with the:**Vision** to inspire innovative MedTech solutions that advance global healthcare, improve patient lives and accelerate Client success and the**Mission** to deliver best-in-class global MedTech development solutions through our people, expertise and technology by adhering to our core**Values:*** Act with integrity in everything we do.* Provide best-in-class customer experiences.* Develop superior talent and deliver expertise.* Respond with agility and provide timely results.* Embrace collaboration, diverse perspectives and ideas. **Compensation Target:** $98,300.00**Job Description:**• Works on assigned studies to ensure that human subject protection is maintained, Good Clinical Practice (GCP), and applicable regulations are followed. • Coordinates and manages clinical site monitoring responsibilities for assigned studies in accordance with contractual agreements, SOPs, and applicable regulatory guidelines. • May conduct on-site and remote site qualification, site initiation, interim, and site close-out monitoring visits. • Serve as primary point of contact for site questions relating to study enrollment, conduct, and close-out issues: liaise with appropriate study team members as needed. • Communicates through verbal and written communication with site investigator and project team overall site performance, trends, deficiencies, and concerns. • Supports study start-up activities such as tracking and performing quality review of study documents, completing, and distributing site activation letters, etc. • Performs study-related training. • Manages the development and maintenance of study documents, processes and systems as assigned. • Ensures quality and completeness of central and site master files. Tracks and maintains required study documents, performs quality control review, manages renewals. • Tracks study site and over all study metrics including but not limited to enrollment, deviations, adverse events, trial master file maintenance. • Attends internal and external meetings as required. • Provides all job-related progress reports and visit documentation as required. • May support safety activities such as narrative writing, managing the CEC/DSMB, etc. • OUS: Prepares and coordinates submissions to regulatory authorities. • May perform other activities as assigned. • Assess the suitability of potential investigative sites through screening interviews, regulatory document review and evaluation of study information and provides input to the site selection process. • Assists with the coordination of the site budget and contract negotiations as directed by the project lead(s). • Assists in preparing sites for audits and in resolving audit action items. • Supports sites during audits remotely and/or onsite as needed. • Participates in meetings with prospective clients. • Supports training and mentoring of CRAs during remote and onsite visits. • Manages the development and/or maintenance of study monitoring plan, templates, trackers, study tools, and site-specific documents. • Assists Clinical Study Manager (CSM) with development of human clinical protocol, investigational plan/brochure, SIV training presentations, and study operations development. • Supports Core Laboratory management and may serve as the primary contact. • Supports data management in CRF development, validation rules, UAT, review data and identify trends, and other reporting/analysis tasks. • Performs and summarizes literature searches. • Registers trials on Clinicaltrials.gov**Qualifications & Technical Competencies:**• Fluency in English and local language, if different, required. • Higher education degree or equivalent education, training, and experience. • Preferred 5 years clinical trial experience. • Preferred 3 years monitoring experience. • Preferred 1 year device trial experience. • Able to work independently once trained. • Good verbal and written communication skills. • Strong organizational skills. • Basic computer proficiency. • Understanding of clinical research processes and regulations. • Certifications such as Society of Clinical Research Associates (SoCRA) or Association of Clinical Research Professionals (ACRP) Certification preferred but not required.**Working Conditions:**• Up to 20% travel for In-House Clinical Research Associates; up to 80% travel for Field Clinical Research Associates. • 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. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. • While performing the duties of this job, the employee is regularly required to talk or hear. The employee is frequently required to stand; walk; sit; use hands to finger, handle, or feel and reach with hands and arms. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, depth perception, and ability to adjust focus. • Extensive use of a computer keyboard. The compensation grade range for this position is:$68,800.00 - $133,700.00-Annual *Please Note: Individual base pay depends on various factors, in addition to primary work location, such as complexity and responsibility of role, job duties/requirements, and relevant experience and skills.*