Project Coordinator , Remote Biosensing Technologies

Medpace Cincinnati , OH 45201

Posted 2 months ago

Apply

This Job is not relevant Tell us why

Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing approximately 3,500 people across almost 40 countries.

Job Summary

Our imaging services are growing rapidly, and we are currently seeking a full-time, office-based Remote Biosensing Technologies Project Coordinator to join our team. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

Responsibilities

Compile and maintain project-specific status reports and project timelines associated with Remote Biosensing Technologies studies;
Maintain inventory of Remote Biosensing Technologies supplies for study sites; and
Interact with study sites and internal associates.

Qualifications

Bachelor's Degree (required) in a health sciences field; or engineering
Prior research related experience is preferred; and
Excellent computer, organizational and communication skills.

Why Medpace?

When you join Medpace, you become part of a team dedicated to supporting the development of ground-breaking drugs and devices. Our employees provide hope for those living with debilitating diseases. We invite you to be a part of something that is impacting millions of people around the globe while enjoying a competitive total compensation and benefits package and internal growth opportunities.

Awards:

Medpace historically named a Top Cincinnati Workplace by the Cincinnati Enquirer
Medpace ranks amongst top CROs for site ratings across all 10 important attributes including CRA training, preparation & organization, accessibility of staff, open communication, and ensuring timely drug availability
Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next:

A member of our recruitment team will review your qualifications and, if interested, you will be contacted for an interview.

EO/AA Employer M/F/Disability/Vets

WARNING: Please beware of phishing scams that offer opportunities with Medpace in exchange for sending money. These scammers pose as legitimate employees from actual companies. Please be advised that a Medpace employee will never ask you for a credit card, send you a check, or ask you for any type of payment as part of consideration for a role with our company. All of our careers require that you first complete an online application and go through some sort of interview process.

Show Full Description

See how you match
to the job

Upload my resume

Download the
LiveCareer app and find
your dream job anywhere

Similar Jobs

View All

Want to see jobs matched to your resume?
Upload One Now!

Project Manager II (IS Technologies Construction Projects)

Cincinnati Children's Hospital Medical Center

Posted 1 week ago

VIEW JOBS SUBFUNCTION DEFINITION: Project manager is responsible for leading an entire project through initiation, planning, execution, control, and completion. REPRESENTATIVE RESPONSIBILITIES * Workflow Facilitate the process of workflow analysis and improvement. Enable groups to define and understand their current workflows and identify areas for improvement or redesign. Coordinate appropriate technical/application resources to provide a thorough understanding of synthesis of changes to systems and processes. Understand the complexity of change management in a large academic health care institution and guide groups to evaluate options that are meaningful and possible. * Project Management Develop and manage project plans, timelines, and activities. Facilitate the maintenance of issue lists, build and decision documentation, meeting minutes, agendas, and status reports as well as other tools crucial to project success. Facilitate cross-functional work teams that include internal employees, technical support, operations personnel, vendor consultants, clinicians, hospital administration and end users. Provide regular project updates and status reports for IS management and ensure timely escalation of issues when necessary. * Customer Service Ensure outstanding end-user support is provided; adhere to and promote continual adoption of change management policies and procedures. Model outstanding customer service behavior, including timely and effective follow-up with customers. Always maintain CCHMC's service standards of being Courteous, Attentive, Respectful and Enthusiastic team members, and Safe (CARES). All other duties as assigned. * Process Improvement Facilitate the process of technology analysis and improvement. Have ability to enable groups to define and understand their current technology profile and their future needs. Work with IS technical resources to define technical criteria for selection of vendor solutions and coordinate vendor selection process. Acquire domain knowledge in order to facilitate the identification and understanding of key project requirements and issues. Recruit expert resources to ensure state of the art technology is presented and evaluated. EDUCATION/EXPERIENCE Required: * Bachelor degree in related field * 2 - 5 years of work experience in a related job discipline Preferred: Master's degree in healthcare administration Unique Skills: Experience with hospital/ healthcare expansion projects

Clinical Project Manager/Clinical Team Lead Rare Disease Remote In USA

Covance

Posted 3 weeks ago

VIEW JOBS Job Overview: Clinical Project Manager/Clinical Trial Lead Rare Disease - Remote in the USA In this role, you will oversee and manage domestic, regional and/or global projects. Responsibilities typically include managing project teams, communications, risk, scope, schedule, cost, quality, and stakeholders effectively ensuring that variance from plan is proactively and effectively mitigated and client expectations are met The Project Manager is expected to have a working knowledge of drug development and clinical trial execution. The Project Manager also compiles and drives documentation for the project, ensuring the accuracy and quality of regulatory data. This role is insourced with the client for a rare disease EAP that has IP using Covance's SOPs/processes and systems (CTMS and eTMF). The selected candidate will be responsible for the oversight of CRAs and liaise with Start Up PM and Pharmacovigilence team and liaise with DM vendor for alignment on monitoring and data cleaning. Will be responsible for study plans, e.g. Communication Plan, Monitoring Plan, Protocol Deviation Plan and vendor management - e.g. central lab, courier for shipment of IP, ISF binders. Additional responsibilities include: * Responsible for project delivery with regards to agreed time, scope, cost and quality * Serve as key client contact for assigned project responsibilities, establishing working relationships with client project teams which result in client satisfaction, operational excellence and thereby increase potential for repeat business * For areas of project responsibility, lead core project team(s) and facilitate team's ability to lead extended project team(s), ensuring effective cross-functional teamwork among project team members including both internal and external Depending on size and scope of project(s), this job duty may be performed in collaboration with a Senior Project Manager and/or Project Director * Serve as escalation point for project issues, within area of project responsibility, to internal and external stakeholders, as appropriate * Proactively identify and resolve conflicts as needed * Understand the project delivery strategy, costing assumptions and resulting budget for assigned project(s) * Monitor project scope, schedule and costs to ensure all remain on track with the contract and with financial performance Initiate and implement appropriate actions to proactively manage the change control process both internally and externally * Proactively lead both quality control and risk assurance activities to ensure project deliverables are met according to regulatory, Covance and client requirements * Create and manage variance to required project Per SOPs, implement and monitor progress against project plans and revise as necessary. Ensure that all staff allocated to assigned project(s) adheres to professional standards and SOPs, providing performance feedback to team member's respective supervisors * Aid in development and maintenance of key project performance indicators for client specified metrics, ensuring that the KPIs are within scope of the project contract * Define and manage project resource needs and establish succession plans for key resources Business Development * In collaboration with relevant departments, prepare and deliver presentations for new business as required * Perform other duties as assigned by management Education/Qualifications: Required: * University/college degree (life science preferred) or certification in a related allied health profession (i.e. nursing, medical or laboratory technology) from an appropriately accredited institution Preferred: * Master or other advanced degree * PMP certification Experience: Minimum Required: * Minimum of five (5) years of relevant clinical research experience in a pharmaceutical company/CRO. * In lieu of the above requirement, candidates with (a) six (6) years supervisory experience in a heath care setting and (b) five (5) years clinical research experience including one (1) years of project management experience (international clinical trial management experience preferred) in the pharmaceutical or CRO industries will be considered * Preferred: Regional project management experience On the Job Experience: * Working knowledge of ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development * Advanced computer skills (e.g., Microsoft Word, Excel, Project, Access and Power Point) * Experience managing projects in a matrix and virtual environment * Excellent communication, planning and organizational skills * Demonstrated ability to lead by example and to encourage team members to seek solutions independently * Demonstrated ability to handle multiple competing priorities and to utilize resources effectively * Demonstrated ability to inspire effective teamwork and motivate staff within a matrix system * Financial awareness and ability to actively utilize financial tracking systems * Working knowledge of project management processes * Ability to work independently and mentor junior project team members * Ability to negotiate and liaise with clients in a professional manner * Ability to present to staff at all levels

Project Environmental Engineer

Psara Technologies

Posted 3 days ago

VIEW JOBS

Apply