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Clinical ink

Associate Project Manager

Clinical ink, Little Ferry, New Jersey, us, 07643


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 plansCoordinating and managing the study change control process from initial request to final decision/approval, including documentation and communicationPlanning and participating in internal and external meetings, including preparing minutes and associated materialsLiaising with internal functional teams and resources to carry out project requirements/tasksLiaising with external teams to achieve project objectives in and around change controls, translations, content development, and integrationsAssisting with managing and updating timelinesCoordinating and working closely with Study Support and Implementation to ensure sites, users, and equipment requests are addressed and entered in a timely fashionPerforming 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 experience1-3 years of clinical trial experience within a Clinical Research Site, CRO or eClinical service provider in a project management role or other equivalent experienceExperience working with clients, ability to communicate to varying levels of personnelExperience working in data collection and management systemsExcellent verbal and written communication skillsExperience working on global projects and cross functional teamsIn depth understanding of clinical trialsWorking knowledge of software delivery lifecycle and methodologyWorking 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#J-18808-Ljbffr