HANDS ON

HANDS ON
Learning & Organizational Development
Est. 1998
Linkedin Instagram X-twitter

Quarterly Learning Programs

TECHNICAL SKILLS

There are many technical skills involved in the work of Life Sciences organizations. Understanding how the business of life sciences works is a great capability to build to enhance your knowledge, impact, and contributions to the business.

Explore our learning programs below...

Please note that each session carries a participant fee of USD 500.00. If your organization has multiple participants, a discounted flat fee may apply. Use sign-up links or please contact us at info@handscom.com for more information.

Access an example Learning Catalog

Technical Skills

  1. AI in life sciences
    AI & Other Trends in Med Tech
    Copy link to share
    (2.5 hours)
    Pretty much all industries are wrestling with artificial intelligence (AI). Learn the latest in AI and other trends in Med Tech.
    2 November from 12:30PM to 3PM Eastern / 9:30AM to 12PM Pacific / 5:30PM to 8PM GMT
    Sign up here
  2. Clinical Operations
    Copy link to share
    (3 hours)
    Learn the fundamentals of Clinical Operations and their role and responsibilities in managing clinical trials and clinical studies. This is useful if you are in Clinical Operations and want more guidance on the full cycle of this group and its work. This is also useful if you work with Clinical Operations and/or just want to learn more about this group’s role in steering clinical trials and clinical studies to successful conclusion.
    2 December from 12:30PM to 3:30PM Eastern / 9:30AM to 12:30PM Pacific / 5:30PM to 8:30PM GMT
    Sign up here
  3. Drug Discovery & Development 101
    Copy link to share
    (2.5 hours)
    This program will help you understand the broader context of Life Sciences’ drug discovery and development, which is important context for all colleagues who work in Life Sciences, as it will help you understand some of the primary functions of Biopharma.
    28 October or 9 December both days at 12:30PM to 3PM Eastern / 9:30AM to 12PM Pacific / 5:30PM to 8PM GMT
    Sign up for October
    Sign up for December
  4. Drug Discovery & Development 201
    Copy link to share
    (2 x 2 hours)
    Learn advanced concepts and principles in drug discovery and development, including key stakeholders across the Biopharma ecosystem, latest trends, and evolutions in Biopharma, and more. NOTE: After you sign-up for the first date, you will receive two Outlook invitations for both parts of this program, since it is a two-part program.
    5 and 12 November (two parts) from 12:30PM to 2:30PM Eastern / 9:30AM to 11:30AM Pacific / 5:30PM to 7:30PM GMT
    Sign up here
  5. GxP
    Copy link to share
    (2.5 hours)
    The Life Sciences and adjacent industries are governed by good, consistent practices. Learn what these are – the full range, organizational requirements and also some of the regulatory reporting requirements.
    6 November from 12:30PM to 3PM Eastern / 9:30AM to 12PM Pacific / 5:30PM to 8PM GMT
    Sign up here
  6. Healthcare Compliance
    Copy link to share
    (2 hours)
    Learn the fundamentals of healthcare compliance pertinent to Biopharma and what organizations must do to remain compliant.
    4 November from 12:30PM to 2:30PM Eastern / 9:30AM to 11:30AM Pacific / 5:30PM to 7:30PM GMT
    Sign up here
  7. Intro to CMC
    Copy link to share
    (3 hours)
    Chemistry, Manufacturing and Controls (CMC) plays a pivotal role across the Life Sciences’ product development lifecycle. If you’re not in a CMC role and want to learn more about what this function does, including where, when and how it is involved in product development progression, this is a great program for you. Whatever your function, we can all benefit from understanding how CMC works, and how we can best interact with CMC and support their role in our organization’s overall success.
    13 November from 12:30PM to 3:30PM Eastern / 9:30AM to 12:30PM Pacific / 5:30PM to 8:30PM GMT
    Sign up here
  8. Market Access 101
    Copy link to share
    (3 hours)
    This program benefits all in Biopharma organizations, as it will give critical foundational information, such as what and who is involved in Market Access, when market access should be contemplated in accordance with product development cycle times. Market access is often addressed too late, which can adversely affect success of Biopharma commercialization.
    13 October from 12:30PM to 3:30PM Eastern / 9:30AM to 12:30PM Pacific / 4:30PM to 7:30PM GMT
    Sign up here
  9. Market Access 201
    Copy link to share
    (3 hours)
    Advance your understanding of the fundamentals of Market Access by advancing your understanding of key constituents, e.g., patients, patients advocates, private and public payers, and more. Understanding what market constituents need will help your organization position itself for optimal market and patient access.
    17 November from 12:30PM to 3:30PM Eastern / 9:30AM to 12:30PM Pacific / 5:30PM to 8:30PM GMT
    Sign up here
  10. Market Access Strategy
    Copy link to share
    (3 hours)
    If you are in a Market Access or adjacent role, such as Sales, Marketing, Medical Affairs, etc., learning how best practice organizations build and deploy market and patient access strategies will help your organization prepare in advance to optimize patient, payer and healthcare provider satisfaction while helping to realize sales and marketing goals as well.
    8 December from 12:30PM to 3:30PM Eastern / 9:30AM to 12:30PM Pacific / 5:30PM to 8:30PM GMT
    Sign up here
  11. Preparing for NDA / BLA
    Copy link to share
    (2.5 hours)
    Learn the primary steps and other considerations when preparing your organization for these critical milestones of New Drug Applications (NDA) and Biologics Licensing Applications (BLA).
    1 December from 12:30PM to 3PM Eastern / 9:30AM to 12PM Pacific / 5:30PM to 8PM GMT
    Sign up here
  12. Regulatory Affairs 101
    Copy link to share
    (3 hours)
    If you’re not in Regulatory Affairs, or brand new to the function, and want to learn more about the fundamentals of how Regulatory Affairs operates in Biopharma, including FDA requirements and various regulatory milestones during product development and product lifecycle management, this program is a great foundation.
    4 November from 12:30PM to 3:30PM Eastern / 9:30AM to 12:30PM Pacific / 5:30PM to 8:30PM GMT
    Sign up here
Return to categories