Peter B Malamis to Lead Life Sciences Group.

Industry veteran Peter B Malamis has been hired as Senior Vice President, Life Sciences of Inteliquet effective immediately.

He leads the group responsible for the sale and delivery of solutions to pharmaceutical and biotechnology companies, contract research organizations (CROs), and other biopharma related groups using patient data. He also oversees the expansion of the company’s life sciences offerings.

With complex clinical trials increasingly the norm, especially in oncology, life science companies and CROs face intensified pressure to implement trials faster, as well as with more precision in their design and recruitment. Inteliquet’s offering enables better trial designs and faster patient identification and enrollment.

“As demand for Inteliquet’s unique digital, data-driven clinical research solutions steadily increases, we’re excited to have Peter lead our efforts in this area,” said Marie E. Lamont, Inteliquet’s Interim President and Chief Operating Officer. “The current pandemic intensified the attention on one of the most intractable problems of our industry: the need for rapid, real-time access to robust patient data that fuels clinical research. Even before now, the scope of required patient data for immunotherapeutic research and personalized drug development challenged trial strategy, design, and recruitment. Peter is a perfect fit with Inteliquet’s heritage and growth strategy. Along with his ‘clinical digital mindset,’ his extensive CRO background and clear understanding of our markets and healthcare partners allow us to move quickly in an environment that changes daily.”

Before Inteliquet, Peter was co-founder and CEO of CRO Analytics, a provider of a cloud-based clinical trial performance system platform. Previously, he was Vice President and General Manager at the MAPI Group, where he helped lead an acquisition that created the largest global CRO devoted to post-marketing research. He was also President of US Operations for the CRO Premier Research and held senior roles at SCIREX (US-focused CRO acquired by Premier), Galt Associates (drug safety and software services), MEDTAP International (health economics and outcomes), and PAREXEL International.

“Clients are seeing that no system can deidentify and normalize electronic medical record data as quickly and accurately as Inteliquet’s solutions,” said Malamis. “More importantly, we can provide the technology they need, but technology alone rarely wins the day. It also takes people who understand the intersection of the technology with the client need to be successful. Inteliquet has a strong, proven foundation of smart, experienced people who never forget their work helps to improve and save lives. We are driven to help our clients and partners overcome challenges as efficiently as possible, so they can bring new therapies to patients as quickly as possible.”

 

Other Executives In the News

Medical Device News Magazinehttps://infomeddnews.com
Medical Device News Magazine provides breaking medical device / biotechnology news. Our subscribers include medical specialists, device industry executives, investors, and other allied health professionals, as well as patients who are interested in researching various medical devices. We hope you find value in our easy-to-read publication and its overall objectives! Medical Device News Magazine is a division of PTM Healthcare Marketing, Inc. Pauline T. Mayer is the managing editor.

Executives on the Move

Dr A Burton Tripathi brings over two decades of Medical Device leadership experience, specializing in developing disruptive technologies, leading commercialization efforts, and facilitating M&A. Having recently served as CEO of TrueVision Systems Inc., he concluded the sale and integration of TrueVision with Alcon.
John Taylor brings more than 30 years of regulatory experience to his role at ELIQUENT, including a distinguished 20-year career at the U.S. Food and Drug Administration (FDA), where he served in multiple leadership positions, including as FDA’s Acting Deputy Principal Commissioner, FDA Counselor to the Commissioner, Acting Deputy Commissioner for Global Regulatory Operations and Policy, and Associate Commissioner for Regulatory Affairs.
Jennifer Riter comes to Kindeva from West Pharmaceutical where she spent the past 27 years in various technical and leadership roles, most recently serving as the Senior Director, Business and Technical Operations.

By using this website you agree to accept Medical Device News Magazine Privacy Policy

Exit mobile version