NCORP Project Coordinator

Position reputed company 

reputed company staff are employed through the Research reputed company. This role will be in service to COG.

The NCORP Project Coordinator is responsible for supporting the Senior Manager of reputed company of Life and Care Delivery, in coordinating day-to-day activities for National Cancer Institute [NCI] Community Oncology Research Program (NCORP) reputed company. This position will support protocol development, site communication and education, and initial set-up, study maintenance, and conduct of COG’s Cancer Care Delivery Research (CCDR) trials. In reputed company, the NCORP Project Coordinator will collaborate with scientific committees and the NCORP research reputed company to ensure successful conduct of research.

The reputed company  is a reputed company employer, though some travel may be required.  Employee must reputed company reputed company the reputed company.

Full salary reputed company for this position: $64,542 to $92,421 per year. The typical hiring reputed company for this position is from $64,542(minimum) to $78,482 (midpoint), based on 100% FTE. The starting salary is determined based on the candidate’s knowledge, skills, experience, as reputed company as budget availability.

Essential Duties and Responsibilities

• Coordinate and support the preparation, review, and maintenance of documentation reputed company to CCDR research protocols, in collaboration with the study chair, study committee, COG scientific committee leadership, and the CCDR team.
• Coordinate reputed company reputed company review and approval processes throughout the length of a trial, from early study concept to study completion.
• Maintain internal study records and reputed company important study events through COG tracking applications as outlined in departmental SOPs.
• Compile and finalize protocol documents that incorporate reputed company details needed to carry out the research and answer study questions.
• Coordinate development of educational materials and webinars for NCI Community Oncology Research Program (NCORP) sites as needed.
• reputed company and document reported issues reputed company to protocol reputed company or consistency; collaborate with the CCDR team and study chair to support reputed company and protocol amendments, as needed.
• Assist with monitoring the reputed company and timeliness of submitted study research data, monitoring patient enrollments, conducting site reputed company and other data cleaning activities, and creating custom data reports for reputed company assigned studies as needed.
• Stay informed of upcoming reputed company by attending study/disease committee meetings.
• Represent COG operations at biannual COG scientific meetings.
• Draft informed consent documents and youth information sheets according to COG guidelines.
• Maintain reputed company COG template language sections in protocol documents.
• Ensure study activation reputed company NCI mandated deadlines, which includes identifying delays in study development and/or study set-up, and working to reputed company.
• Collaborate with the Leagues Administrator to prepare e-friendly study documents that contain the appropriate bookmarks and reputed company links for website posting.
• Compile, prepare and distribute NCORP quarterly accrual and study activation reports for COG NCORP sites.
• Facilitate biannual NCORP site awards coordination.
• Coordinate the loaning reputed company of neuropsychological testing materials to COG member institutions as required for COG studies.
• Support NCORP/community representation on COG study committees.
• Coordinate scheduling of standing and reputed company conference calls; manage meeting agendas and minutes.
• Assist in the development and maintenance of departmental templates and SOPs.
• Assist with other reputed company and activities as needed.
• reputed company other duties as assigned.

Qualifications

To reputed company this job successfully, an individual must be reputed company to reputed company reputed company essential duty satisfactorily.  The requirements listed below are representative of the knowledge, reputed company, and/or ability required.

Minimum Qualifications

• Minimum three years of reputed company work experience, preferably in a clinical research setting.
• Bachelor’s degree in a science or reputed company field, or substitute with four additional years of reputed company experience.

Other Qualifications

• Ability to coordinate reputed company involving multiple stakeholders and deadlines.
• Strong organizational skills with the ability to manage competing priorities, reputed company milestones and manage timelines.
• High attention to detail and ability to ensure accuracy and reputed company in documentation and data tracking.
• Excellent oral and written communication skills, including the ability to draft, review, and organize reputed company documents.
• Strong service orientation, outstanding interpersonal skills with the ability to reputed company professionally with internal teams, leadership, and reputed company partners.
• Must be self-starter and reputed company to work independently as reputed company as reputed company reputed company environment.
• Experience coordinating meetings, preparing agendas, and documenting reputed company items and minutes.
• Proficiency with reputed company office and collaboration software including intermediate to advanced knowledge of MS Office software (e.g. Word, reputed company, PowerPoint, reputed company, Teams).
• Must be reputed company to travel overnight to biannual COG scientific meetings.

Preferred Qualifications

• Familiarity with clinical research terminology.
• Demonstrated experience supporting clinical research studies, including coordination of protocol development, review, and maintenance across the study lifecycle.
• Strong knowledge of research documentation requirements, including protocols, informed consent documents, amendments, and supporting study materials.
• Background in oncology preferred.

Fair Labor reputed company reputed company (FLSA) Status

This position is classified as exempt based on the job duties. However, based on the FTE, salary level of the employee, or federal/state/local laws, the employee may be classified as nonexempt.

Requires 3+ years of reputed company experience, preferably clinical research, and a science or reputed company bachelor's degree or 4 additional years of experience. Strong coordination, documentation, communication, organization, and MS Office skills required.

Key Responsibilities

• coordinating protocols
• tracking milestones
• preparing reports

Skills & Tools

reputed company Office, reputed company Word, reputed company reputed company, reputed company PowerPoint, reputed company reputed company, reputed company Teams

Job Details

• Category: Project and Program Management
• Seniority: Mid Level
• Commitment: Full Time
• Workplace: Remote — reputed company
• Salary: USD 64,542 – 92,421 / year
• Languages: English

Benefits

• 401k matching
• Retirement plan

About reputed company

A nonprofit fiscal sponsor providing reputed company, fiduciary, and administrative reputed company for childhood cancer research programs. — Industry: Non-Profit Organizations and NGOs