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HomeResearch & DevelopmentClinical Research Project Management – 7 Breakthrough Behaviors For Success

Clinical Research Project Management – 7 Breakthrough Behaviors For Success

Teachers
Dalfoni Banerjee
Category:
Clinical Trials (GCP Training)/ Leadership & Training/ Live Webinars/ Research & Development/
Clear
Duration: 90-Minutes
January 14, 2020 | 1 PM EST
includes handouts
  • Description
  • Who Should Attend
  • What To Expect

Description

COURSE DESCRIPTION

OVERVIEW

As a Clinical Project Manager (CPM), you confront myriad tactical challenges that can be all-consuming and result in you spending a considerable amount of your time “firefighting”.  These setbacks don’t allow for much – if any – time to conduct a trial from a birds-eye view.  Timelines are always too tight, so a concise, metered approach based on thought-out processes and consistent behaviors is your best bet to ensure less-stressful clinical operations.

Many of us have decent, foundational, clinical project management processes in place.  It is the behaviors that need to change.  Are you prioritizing your work?  Are you ensuring your actions actually prevent roadblocks, setbacks, and wasted time?  Believe it or not, there are seven (7) breakthrough behaviors that can help you achieve the goal of a “stress-mitigated trial.”

This interactive, 90-minute session will provide a roadmap for:

  • A strategic plan for trial management
  • Immediate implementation of a set of behaviors that prevent or mitigate “fire-fighting,” which will make you and your colleagues more productive

 

LEARNING OBJECTIVES

By attending this session, you will learn:

  • Specific approaches that can boost your efficiency and effectiveness…regardless of process or organizational framework
  • Tried-and-true techniques to help you avoid the many pitfalls of clinical project management
  • Real-world examples that demonstrate how embracing the “7 behaviors” mitigate “firefighting.”
  • Why it’s a win-win for organizations to cultivate a framework that embraces these behaviors

Who Should Attend

WHO SHOULD ATTEND

This course will be of benefit to clinical trial managers or those looking to work in a clinical project management role. Additionally, anyone who currently manages projects within the clinical development arena and associated functional areas will find this training very beneficial. This includes personnel in:

  • Clinical Research
  • Clinical Operations
  • Monitoring
  • Quality
  • Other functions that require either project management or driving processes with large and/or cross-functional teams

What To Expect

WHAT TO EXPECT

HOW TO PARTICIPATE

This webinar will be offered live. With your course purchase, you may participate live or view the recording at your convenience (available for 30 days). Access instructions for the live viewing will be emailed to you 3 business days prior to the scheduled date. Access to the recorded version will be available 1 business day after the live course has run.

To access the course, you need only a telephone and computer with internet access.

This webinar is scheduled for live instruction on
Date: January 14, 2020
Time: 1:00 – 2:30 PM EST

Choose to participate live or listen to the recording afterward!

THE TRAINING PLATFORM

Our webinar platform combines the convenience of online training with the live interactivity of the classroom. Quizzes, case studies, break-out sessions, and assessments are often incorporated into the training . Other ancillary materials can be downloaded from the “Handouts & Resources” area in the virtual classroom. Each course purchase includes a completion certificate issued to the participant after the course.

USER AGREEMENT

Your registration fee for a single participant entitles you to one telephone dial-in and one online course log-in per site. Course testing capabilities, stored results for training records, and completion certificates are available for only one registrant per single participant course purchase. For multiple participants, please purchase more than one registration or consider our 5 or 10 participant packages.

The recorded version of the training will be available for 30 days after purchase.

Is this course right for me? We’d be happy to help you select the right training course to meet your needs.
Give us a call at 215-675-1800 and use Option 3 (9am – 5pm EST, M-F) for assistance.

About Instructors

Dalfoni Banerjee
Dalfoni Banerjee is an award-winning, solution-focused entrepreneur. Beginning her career over 25 years ago in academic, pharmaceutical, and biotechnology research laboratories, she went on to lead inspection-readiness efforts, drive clinical research and clinical operations, manage relationships between pharma and key opinion leaders, develop marketing strategies/tactics, and launch new drug products – across 12+ therapeutic categories

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Clear
Duration: 90-Minutes
January 14, 2020 | 1 PM EST
includes handouts

CATEGORIES

  • Sales & Marketing (1)
  • Clinical Trials (GCP Training) (99)
  • Manufacturing (GMP) (88)
  • Medical Device Training (55)
  • Quality (39)
  • Regulatory & Compliance (197)
  • Research & Development (70)
  • Leadership & Training (36)
  • IT & Data Integrity for Pharma (31)
  • Live Webinars (8)
  • On-Demand Courses (220)
  • Introductory Pharma Courses (19)
  • Special Packages (5)

TOPICS

Cleaning Validation Cleanroom Clinical Trials Cloud CMOs Computer Systems CRAs CROs Data Integrity Device eCTD EHRs EMA Equipment Facilities FDA GCP GDP GLP GMP HIPAA Human Error ICH Informed Consent Inspections Instructional Design Management manufacturing Marketing MDR microbial control Process Validation Project Management Quality Quality by Design Quality Risk Management Remote Monitoring Risk Risk-Based Monitoring Root Cause Analysis Site Monitoring SOPs Training Trial Master File Upcoming Courses

Your Courses

Upcoming Live Courses

  • Clinical Research Project Management - 7 Breakthrough Behaviors For Success
  • The MHRA Data Integrity Guidance Clarified: What it Means for Industry & Patients
  • Implementing a Robust Change Control Program – Key Elements for Process and Documentation Compliance
  • Responding to Clinical Observations: Developing Robust Audit & Inspection CAPAs
  • CAPA and Root Cause Analysis: Essentials Post ICH GCP E6 (R2) Addendum
  • Medical Device Recalls – Keys To Implementing A Successful Approach
  • Understanding Aseptic Technique and Cleanroom Behavior – Avoiding Human Error

Contact

  • 101 Gibraltar Road, Suite 100 Horsham, PA 19044
  • 215-675-1800 (option 3)
  • info@lifesciencetraininginstitute.com
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