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Clinical Project Coordinator (Remote)

LensaDurham, NC
yesterday
Remote

Company

Lensa

Location

Durham, NC

Work Schedule

full time

Work Location

remote

Job Description

The Clinical Project Coordinator (Remote) at Lensa supports biotech/pharma clinical trials by managing timelines, documentation, and cross-functional teams from Durham, NC. Ideal for organized professionals with clinical research experience seeking flexible remote work.

Full Description

Job Overview: Lensa, a leading player in the biotech and pharmaceutical industry based in Durham, North Carolina, is seeking a skilled Clinical Project Coordinator to join our dynamic team on a remote basis. This pivotal role involves overseeing clinical trial projects from inception to completion, ensuring compliance with regulatory standards, and driving operational efficiency in a fast-paced environment. As a remote position, it offers flexibility while contributing to groundbreaking advancements in healthcare innovation. Key Responsibilities: Coordinate all aspects of clinical project timelines, including planning, execution, and monitoring to meet milestones and deliverables. Liaise with cross-functional teams such as clinical operations, data management, regulatory affairs, and investigators to facilitate seamless communication and problem-solving. Maintain accurate project documentation, including study protocols, budgets, and progress reports, while ensuring adherence to FDA, ICH-GCP, and other applicable guidelines. Track project risks, budgets, and resources, implementing corrective actions as needed to mitigate delays. Prepare and present status updates to senior management and stakeholders, utilizing tools like MS Project or similar software. Support site initiation, patient recruitment strategies, and close-out activities to ensure high-quality data collection and trial success. Foster vendor and CRO relationships to optimize external collaborations. Required Qualifications: Bachelor's degree in life sciences, nursing, pharmacy, or a related field; advanced degree preferred. Minimum of 3-5 years of experience in clinical research coordination or project management within biotech/pharma. Proven track record in managing Phase I-IV clinical trials. Strong knowledge of clinical trial regulations (FDA, EMA) and GCP principles. PMP certification or equivalent is highly desirable. Skills: Exceptional organizational and multitasking abilities with keen attention to detail. Proficient in project management software (e.g., MS Project, Asana, Smartsheet) and Microsoft Office Suite. Excellent verbal and written communication skills for stakeholder engagement. Analytical mindset for risk assessment and data interpretation. Ability to thrive in a remote setting with high autonomy and virtual collaboration tools like Zoom, Slack, and Teams. Problem-solving prowess and adaptability to evolving project needs. Company Info: Lensa is at the forefront of biotech innovation in Durham, NC, a hub for life sciences research. We specialize in developing novel therapies for unmet medical needs, partnering with top-tier institutions and fostering a culture of excellence, collaboration, and employee growth. Benefits: Competitive salary package with performance-based bonuses. Comprehensive health, dental, and vision insurance. Generous PTO, remote work stipend, and flexible hours. 401(k) matching and professional development reimbursement. Growth Opportunities: Advance to Senior Project Manager or Clinical Operations Lead roles. Access to ongoing training in emerging therapies and leadership programs. Opportunities for cross-departmental projects and industry conference attendance to expand your network and expertise.

Key Skills

Clinical Trial ManagementProject CoordinationGCP ComplianceRegulatory KnowledgeStakeholder Communication