Oncology Project Manager

March 14

🧀 Wisconsin – Remote

Although this job is listed in Wisconsin, this company may be open to hiring remote in other states.

⏰ Full Time

🟢 Junior

🟡 Mid-level

👷‍♀️ Project Manager

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MERIT CRO

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MERIT CRO is a global scientific and clinical research organization specializing in ophthalmology, oncology, respiratory, and neurology therapeutic areas. They provide comprehensive clinical trial services, including endpoint management, quality assurance, and advanced imaging analysis through their proprietary EXCELSIOR™ technology platform. With a focus on delivering high-quality data and reducing variability, MERIT collaborates closely with pharmaceutical and biotech companies to accelerate product development and improve therapeutic options globally. Their expertise in managing complex imaging studies, particularly in ocular diseases and spirometry, positions them as a key partner in advancing clinical research.

Ophthalmology clinical trials • corneal endothelial cell count • optical coherence tomography • technician and equipment certification • imaging CRO

51 - 200 employees

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

💰 $600k Seed Round on 2016-08

📋 Description

• Manage office tasks including organization and coordination of controlled documents • Assist in development of project and regulatory documents; includes proofreading of documents • Respond to quality review audits and clearly document responses to facilitate resolutions • Assist with the development/implementation of training programs • Monitor own work to ensure quality and completeness • Perform and oversee all study activities from start-up through close out and data lock • Organize and prioritize work assignments to complete assignments and tasks on time and with quality, and has the ability to anticipate problem areas in advance • Apply creative approaches and ideas to solve problems maximizing effective use of appropriate resources • Prepare study start up materials, organize and conduct internal study start up meeting, and follow up on action items • Establish and maintain routine communication among internal MERIT departments, sponsors, site staff, and other designated parties • Initiation of Master Project File and maintenance of project documents • Establish study files and create and distribute study documents • Attend project meetings internally and with sponsor (via teleconference or face-to-face) throughout the project • Independently process clinical data from start up through database lock prioritizing work to meet project timelines • Responsible for assisting in all aspects of study conduct, initiation through closeout

🎯 Requirements

• Minimum of a Bachelor’s degree in a health related, biological science, computer science, data entry, customer service or business management is preferred, or an equivalent combination of education, training, and work experience. • A minimum of two (2) years of clinical trial or project management experience in a related field. • Strong interpersonal and organizational skills, excellent attention to detail, ability to follow direction, assess Company needs and work independently. • Computer skills to include proficiency in Microsoft Office software and ability to learn Company specific software. • Must be able to project a professional attitude and image appropriate for the work environment. • Ability to participate and contribute in a team environment as a team member. • Oral and written communication is clear, concise, and effective.

🏖️ Benefits

• 401(k) • Dental insurance • Disability insurance • Health insurance • Life insurance • Paid time off • Vision insurance