Clinical Study Nurse Coordinator Jobs in Arkansas

Act with integrity in everything we do.

Develop superior talent and deliver expertise.

Respond with agility and provide timely results.

Embrace collaboration, diverse perspectives and ideas.

Come and work for an organization with the:

Note that vendor management is not limited to the CRO, but includes ancillary vendors (e.g. translations, trial insurance, and central laboratory).

Ensure DS internal tracking systems are updated (e.g. Global Project Management System, GPMS).

Education Qualifications (from An Accredited College Or University)

Associate degree or with a nursing diploma with substantial experience preferred.

4 or More Years relevant experience is required with a BS preferred.

Bachelor's Degree in the Sciences preferred.

Oversee data collection, management, and entry into study databases, ensuring accuracy and completeness

Strong knowledge of clinical research processes, regulations, and guidelines.

Excellent organizational, communication, and interpersonal skills.

Collaborate with study teams to develop and implement study protocols, ensuring compliance with regulatory guidelines and ethical considerations

Coordinate participant recruitment and enrollment activities, including screening, selection, and informed consent processes

BA/BS degree in a relevant subject

Co-manages maintenance of the centralized Informed Consent Form mailbox.

Minimum of three years of relevant experience in the biopharmaceutical/CRO industry.

Ability to manage multiple tasks simultaneously and meet deliverables in accordance with stated timelines.

MUST CURRENTLY WORK AT A CRO/PHARMA

Reviews and validates quality and accuracy of Informed Consent Form templates.

Supports development of Informed Consent Form templates.

Management experience of CROs, Vendors and Consultants preferred

Ensures the competencies and skills required for the Clinical team is consistent with the company defined requirements

Mentor junior team members to support development by delegating responsibilities, overseeing and supporting development plans

8+ years progressive experience in clinical operations preferably within the biotech, pharmaceutical, and/or CRO environment

Possess understanding of treatment landscape, standard of care, upcoming approvals, and good knowledge of KOLs and investigators

Experience developing trial plans including site monitoring, pharmacy and lab manuals, risk mitigation strategies, trial budgets and site selection/feasibility as required

Support the organization with daily tasks including user management, site management, equipment requests, data entry and report generation

Provide support for front-end client activities across multiple clinical research studies

Work closely with clients to ensure all data required for study start-up is collected and maintained

Provide details and information to clients in response to inquiries regarding study support and set-up

Update project-related internal databases and electronic files to ensure accuracy

Assist with special department projects

Must have excellent management and communication skills (written and verbal), strong problem-solving skills, and be detail oriented

Manages vendors, including the implementation and coordination of vendor’s Scope of Work (SOW).

Manages study budget and timelines. Identifies, resolves, or escalates issues involving study timelines and deliverables

Relevant experience as a CRA preferred

Study planning and set-up, maintenance, and close-out experience.

Must have a solid understanding of clinical research operations including GCP and regulatory requirements and operational procedures

Minimum of 3-5 years of project management experience in the pharmaceutical industry, with a focus on clinical study management

PMP or similar project management certification is preferred

Collaborate with cross-functional teams, including clinical operations, data management, biostatistics, and quality assurance, to ensure seamless study execution

Familiarity with Veeva or other relevant clinical trial management systems

Veeva or similar study management platform

Study Project Manager - 100% remote