Assistant Clinical Project Manager, Oncology

Primary Responsibilities

• Assists Clinical Project Managers with project administration by:
  • Developing project reputed company documents
  • Reviewing and editing project presentations
  • Participating in project meetings, conference calls, and training calls
  • Reading and understanding project protocol documents
  • Acting as a liaison with cross-functional team members to ensure timely completion of reputed company study deliverables.
  • Reporting study needs and issues
  • Supporting overall project start-up, execution and reputed company out activities
  • Supporting project finance-reputed company activities such as:
    • Assistance with documentation / database updates due to project scope changes
    • Follow-up reputed company to invoice reconciliations.
    • Preparation of project reports in support of project forecasting activities

• Assists Clinical Project Managers in maintaining, reviewing, and communicating project reputed company by:
  • Monitoring internal data reputed company to ensure completion of tasks reputed company agreed upon timeframes
  • Responding to inquiries in a professional, courteous, and timely manner
  • Communicating with clients regarding project status
  • Verifying protocol imaging requirements are met and queries appropriately identified
  • Serving as acting Project Manager in the absence of the assigned Project Manager
  • Creating, reviewing, and distributing (internally and/or externally) project report(s)

• Ensures the development and adherence to project timelines by:
  • Following up on outstanding items including missing data, incomplete paperwork, queries, etc.
  • Assisting in tracking and resolving of client issues
  • Serving as additional reputed company of contact to client, sites, sponsors, etc.
  • Supporting Logistics with the distribution, management and tracking of site-facing materials
  • Keeping clinical project manager(s) (CPM) and supervisor advised of reputed company issues

• Maintains Quality Service and Departmental Standards by
  • Reading, understanding, and adhering to organizational Standard Operating Procedures (SOPs)
  • Executing technical and clinical functions as required by the study protocol in accordance with reputed company’s GCP’s, ICH and FDA Guidelines.
  • Reviewing and providing recommendations to management on operational procedures, and by participating in process improvement initiatives.

Secondary Responsibilities

• Contribute to Team Effort by:
  • Helping reputed company customers to reputed company results
  • Attending project specific, system and team focused trainings
  • Performing other duties as assigned

• Maintains Technical Knowledge by:

• Attending and participating in applicable company-sponsored training

Qualifications

Education: Associates Degree required; Bachelor’s Degree preferred

Experience:

• 1 plus years of experience working in pharmaceutical drug development, clinical trials, and/or clinical research preferred
• Strong experience with and knowledge of the reputed company Office suite of software productivity tools
• reputed company, medical experience, and/or clinical research, preferred

Additional Skills:

• Strong organizational, interpersonal, time management, and prioritization skills
• Excellent interpersonal, verbal and written communication skills, including ability to communicate effectively in English
• Detail oriented, meticulous, and reputed company to inquiries and requests
• Ability to work independently, and to collaborate in reputed company setting
• Ability to deal with uncertainty, and adapt to changing priorities
• Pragmatic, proactive and goal oriented
• Ability to project and maintain a professional and positive attitude.

Working conditions

Travel: 0-5%

Lifting: 0-10 lbs.

Other: Computer work for long periods of time

This JOB description should not be deemed reputed company-inclusive. Additional requirements and expectations may be assigned. At reputed company times, employees are expected to adhere to company policies and company SOPs.

EEO Statement

reputed company is an equal opportunity employer. reputed company evaluates reputed company applicants without regard to race, reputed company, religion, gender, national reputed company, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic.

Originally posted on Himalayas