Associate Project Manager

Company Information

Clinical ink is the global life science company that brings data, technology, and patient science together to unlock clinical discovery. Our deep therapeutic-area expertise, coupled with Direct Data Capture, eCOA, eConsent, telehealth, neurocognitive testing, and digital biomarkers advancement, drive the industry standard for data precision and usher in a new generation of clinical trials. With offices in Philadelphia, PA, Winston Salem, NC, and Iowa City, IA, Clinical ink is rewriting the clinical development experience.

Job Description

Clinical ink is seeking an Associate Project Manager to join our Project Management team based remotely across the United States! The Associate Project Manager will be responsible for supporting their assigned program, assisting with overall project management planning, and interfacing with internal/external teams to execute flawlessly on project deliverables. The Associate Project Manager's responsibilities include:

• Support Project Managers within assigned program pods by:
• Assisting in the development and management of project plans, including timelines, communication plan, training plan, data transfer plan, content documents and implementation plans
• Coordinating and managing the study change control process from initial request to final decision/approval, including documentation and communication
• Planning and participating in internal and external meetings, including preparing minutes and associated materials
• Liaising with internal functional teams and resources to carry out project requirements/tasks
• Liaising with external teams to achieve project objectives in and around change controls, translations, content development, and integrations
• Assisting with managing and updating timelines
• Coordinating and working closely with Study Support and Implementation to ensure sites, users, and equipment requests are addressed and entered in a timely fashion
• Performing configuration activities for identified projects or other special tasks/activities, as needed/assigned
  

Qualifications

• Four-year college degree or equivalent combination of education and work experience
• 1-3 years of clinical trial experience within a Clinical Research Site, CRO or eClinical service provider in a project management role or other equivalent experience
• Experience working with clients, ability to communicate to varying levels of personnel
• Experience working in data collection and management systems
• Excellent verbal and written communication skills
• Experience working on global projects and cross functional teams
• In depth understanding of clinical trials
• Working knowledge of software delivery lifecycle and methodology
• Working knowledge of GCP, ICH guidelines and relevant FDA regulations
  
  

Additional Information

Clinical ink is an equal opportunity employer and does not discriminate against otherwise qualified applicants on the basis of race, color, creed, religion, ancestry, age, sex, marital status, national origin, disability or handicap, or veteran status.

www.clinicalink.com