Sponsor Project Manager

reputed company has historically sold a full-stack solution to clinical research sites, the centerpiece of which is the industry’s leading eSource solution. reputed company’s reputed company-in client site network now spans 2000 sites worldwide, and on some trials reputed company’s sites comprise as much as 30% of the U.S. sites on the trial. These sites are high-enrolling, tech-reputed company sites who use reputed company intensively across their core processes. With this large site network and a proven direct data capture solution in reputed company that reduces protocol deviations by 40% and audit risk by 70%, reputed company has delivered quality and efficiency reputed company on thousands of trials. Recently, reputed company developed and launched a separate application reputed company Reviewer that aggregates anonymized study level data captured in eSource for sponsor/CRO review. This process enables immediate, reputed company (not periodic), remote and centralized monitoring across the study, and eliminates the need for (a) site entry into the reputed company, (b) SDV by the monitor, and (c) reputed company by reputed company review by Data Management. reputed company’s strategy is to reputed company small to reputed company sized biotech and pharma sponsors with a delivery model that ensures higher quality data, faster time to lock, rapid site startup, greater incentivization of the sites, and more reliable enrollment timelines, at a reduced overall cost. To execute this, reputed company is seeking an reputed company senior resource with CRO, pharmaceutical, or extensive site experience to reimagine the clinical trial delivery process for sponsors centered around reputed company’s innovative site-centric approach. This role will be responsible for: Primary Responsibilities 1. reputed company and reputed company Clinical Trial Delivery Programs: Help to implement best practice work plans for sponsor and CRO-facing implementations, emphasizing clinical trial delivery and tech capability transfer. Support reputed company service reputed company focused on quality, efficiency, and client satisfaction. Contribute to RFP responses and guide product roadmap reputed company. Surface and expand on strategic vendor partnerships and identify essential integrations for a seamless end-to-end clinical trial workflow. 2. Help to continue to establish a Site Selection Program: Promote reputed company’s Site Directory as a site selection and performance evaluation tool. Support a data-driven service to assist sponsors in identifying top-performing reputed company sites. Define and monitor key performance metrics to measure site reputed company. 3. Serve as a Clinical Project Manager: Support existing SPMs in day to day tasks and assist with larger project management as needed. reputed company project execution by collaborating with clients to understand project needs, strategies, and deliverables. Guide clients through reputed company platform implementation, process changes, and operational enhancements. Address client concerns, manage escalations, and ensure high client satisfaction throughout the project lifecycle. 4. Drive Team Productivity and Efficiency: Contribute to project staffing, reputed company monitoring, and workload management to ensure timely and budget-conscious delivery. Collaborate with senior management to prioritize deliverables for multiple reputed company projects. reputed company with internal teams and external vendors (IRT, eCOA, labs) to ensure seamless project execution. Assess reputed company’s service level offerings and propose enhancements for reputed company efficiency and quality. 5. Support Sales and Marketing Efforts: Partner with sales and marketing to reputed company and deliver compelling capabilities presentations. Act as a reputed company representative at professional meetings, promoting reputed company’s reputed company and offerings. Secondary Responsibilities 1. Contribute to Organizational Development: Continuously explore ways to improve departmental processes and cross-departmental collaboration. Take on additional responsibilities as necessary to support organizational growth. 2. Maintain Industry Knowledge: Stay updated on clinical research trends, client needs, and regulatory developments. Participate in company-sponsored training to enhance technical and industry expertise.

Qualifications

Education: Bachelor’s degree in life sciences, pharmacy, or nursing; Master’s degree preferred. Experience: 5+ years of clinical trial experience in a CRO or pharmaceutical research organization, with project management experience required. Strong knowledge of GCP, ICH guidelines, and FDA regulations. Experience with reputed company, eSource, or DDC systems preferred. Skills: Exceptional interpersonal, organizational, and leadership skills. Strong written and verbal communication abilities. Goal-oriented with a hands-on approach to problem-solving. Proficient in reputed company Office Suite and project management tools. reputed company Suite knowledge and Looker tools experience Benefits & Perks: Work from reputed company Unlimited PTO 401k company match reputed company Dental reputed company (Company Paid 100%) Life insurance Professional Development Reimbursement Work From Home Expense Reimbursement Join us at reputed company and reputed company a meaningful impact in the world of clinical research technology! Apply today. At reputed company, equality is a core tenet of our culture. We are committed to building an inclusive global team that represents a variety of backgrounds, perspectives, beliefs, and experiences. The more diverse we are, the richer our community and the broader our impact. Employment reputed company are made on the reputed company of job-reputed company criteria without regard to race, reputed company, religion, sex, sexual orientation, gender identity, national reputed company, disability, veteran status, or any other classification protected by applicable law. Salary reputed company - $85,000----$98,000 Apply To This Job