Risk Mitigation for Oncology Clinical Trials

Life Sciences, Clinical Trials, Patient Recruitment & Retention,
  • Tuesday, May 18, 2021 | 1pm EDT (12pm CDT / 10am PDT)
  • 60 min

Since early 2020, the oncology clinical trials industry made rapid changes in order to ensure mission critical operations continued to protect participant rights, privacy, safety and data integrity. Particularly at clinical sites, research teams have had to restructure their team and operations according to institutional directives to prevent the spread of COVID-19 while continuing to offer trial options to patients, with some regions more deeply affected than others.

In this webinar, Julie Martin, CEO & co-Owner of Scimega Research, presents on key areas of risk in critical oncology clinical trial operations, with mitigating tactics & strategies to build resiliency in 2021-2022 and maximize clinical development progress.

Register for this webinar to explore critical clinical trial operations mitigating tactics & strategies for prevention, recovery and resiliency in 2021-2022, and learn more about:

  • Key risk areas of greatest concern in oncology clinical trials
  • Strategies used to mitigate threats in 2020 for small & mid-size U.S. oncology biotechs: what worked and what didn’t
  • Cutting-edge small & mid-size oncology biotech trials: where to run them and which aspects may be different moving forward
  • What decision factors are expected to most influence your choice of region(s) in 2021-2022. Ex: speed of start-up, participant diversity, regional participation rates

Bonus Offer: Register now and receive immediate access to the white paper Expert Guidance to Key Advantages of Canadian Regulatory Landscape.

Speaker

http://Julie%20Martin,%20Scimega

Julie Martin, CEO & Co-owner, Scimega

Julie joined Scimega 8 years ago. Having worked for 2 other CROs before, her passion for Scimega’s business and team stems from knowing its expert oncology clinical development services add distinct value to industry stakeholders at a time when it’s needed most.

As CEO, Julie’s vision is to secure the company’s long-term success by leveraging her in-depth industry expertise & business acumen. She equates that success with setting a clear vision for the organization’s continued sense of purpose. Julie is responsible for developing successful business strategies & leveraging industry opportunities, all of which support the common vision she shares with her team.

Her leadership & collaboration with the managing Board of Directors ensure the business excellence upon which Scimega has built its reputation. Julie plays a vital role in promoting Scimega’s expertise and showcasing Canada’s attributes as a formidable partner in global oncology drug development.

Message Presenter

Who Should Attend?

Clinical operations team leaders from small to mid-size biotech and biopharma companies managing complex oncology clinical studies will find the most benefit from this webinar. Relevant job titles include:

  • Manager/President/Director of Operations
  • Director Regulatory Affairs
  • CEO
  • CMO

What You Will Learn

In this webinar, participants will learn about:

  • Key risk areas of greatest concern in oncology clinical trials
  • Strategies used to mitigate threats in 2020 for small & mid-size U.S. oncology biotechs: what worked and what didn’t
  • Cutting-edge small & mid-size oncology biotech trials: where to run them and which aspects may be different moving forward
  • What decision factors are expected to most influence your choice of region(s) in 2021-2022. Ex: speed of start-up, participant diversity, regional participation rates

Xtalks Partner

Scimega

Scimega is a Canadian only, oncology only CRO with a depth of expertise in the region that sets us apart. This is why our U.S. clients engage Scimega – to help them successfully conduct their trials in Canada. This is our niche. We only work with cutting-edge small and mid-size U.S. biotechs that wish to expand their global oncology clinical trials to Canada. Without this specific interest this webinar is not for them.

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