Clinical Trial Asst Proj Manager--Benign Heme ; Cancer Center Protocol Office
Massachusetts General Hospital(MGH)

Boston, Massachusetts

Posted in Health and Safety


This job has expired.

Job Info


GENERAL SUMMARY/OVERVIEW:

The Associate Manager works under direct supervision of a more experienced manager. The Associate Manager provides first-line supervision to research staff members and oversees the day-to-day operations of the staff while maintaining some data management responsibilities and a working knowledge of all aspects of clinical research data management.

PRINCIPAL DUTIES AND RESPONSIBILITIES:

Management responsibilities will include the following

  • Provide first-line supervision to a minimum of 4-6 FTEs and/or assist with department-wide specialized projects
  • Facilitate new hire, correction action, and performance evaluation process for research staff
  • Train new staff and assess continuing education needs
  • Assist staff with task prioritization for project assignments by meeting regularly and maintaining meeting documentation
  • Manage staff productivity and quality of work produced by assessing work effort on individual studies
  • Work with sponsors to resolve monitoring issues

Management responsibilities may include the following
  • Work with the Clinical Research Manager or Director to identify changes associated with Standard Operating Procedures and develop processes to ensure compliance
  • Assist with pre-activation activities including pre-site qualification visits, SIVs, and facility tours
  • Assist investigators with the completion of the New Protocol Intake Sheet for regulatory routing
  • Proctor meetings, supply meeting materials and develop group-specific tools

Data management responsibilities may consist of the following:
  • Verify patient eligibility via chart abstraction and analysis of case data
  • Collect and interpret data necessary for enrollment; register patients
  • Implement and monitor procedures to ensure protocol compliance
  • Manage data collection via chart abstraction and submit data in timely fashion
  • Monitor and report adverse events as required by institutional/federal regulations
  • Resolve data discrepancies
  • Prepare IRB submission of protocol revisions, safety reports, annual progress reports
  • Assess impact of new risk information on consent documents and revise appropriately
  • Organize and attend on- and off-site Investigator meetings to establish procedures
  • Organize and prepare for monitoring visits and both internal/external audits


Qualifications
SKILLS/ABILITIES/COMPETENCIES REQUIRED:
  • Demonstrated time management and organization skills
  • Strong written and verbal communication skills
  • Knowledge of current and developing clinical research trends
  • Sound interpersonal skills
  • Ability to work independently and display initiative
  • Demonstrated ability to successfully manage multiple projects
  • Established rapport with investigators and sponsors with the ability to resolve operational matters within a disease group
  • Potential to effectively supervise and train staff
EDUCATION:
  • BA/BS degree required

EXPERIENCE:
  • 2-3 years research experience required
  • Prior experience within the Cancer Center Protocol Office (CCPO) preferred
SUPERVISORY RESPONSIBILITY:
  • Orient and train new staff and may supervise a minimum of 4-6 FTEs
WORKING CONDITIONS:
  • Duties will be performed in an office setting


EEO Statement
Massachusetts General Hospital is an Equal Opportunity Employer. By embracing diverse skills, perspectives and ideas, we choose to lead. Applications from protected veterans and individuals with disabilities are strongly encouraged.


This job has expired.

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