DSP

DSP is a full service CRO that manages Phase I-IV clinical studies for small to mid-sized pharmaceutical, biotech, and device companies from study setup through NDA submission.

About Us

Our Team

DSP functions with a lean but very efficient team of approximately 30 employees located in our Parsippany office. Our monitors are all regionally based and located throughout the US and Canada. We act as an extension of your company, and you'll come to think of our staff as your own employees.

We are proud of a very low turnover rate amongst our staff, creating greater study continuity, fewer learning curves, lower training costs, and lower overall study costs.

Because we're a small CRO, senior executives are very accessible and we value open, direct lines of communication with our clients.

Your assigned Study Manager is your decision maker!

Management

Darlene Panzitta

Darlene Panzitta, President/Founder

Darlene has been working in the pharmaceutical industry for over 13 years. Prior to founding DSP, she worked as a Manager of Clinical Development at Berlex Laboratories. While at Berlex, she was responsible for the overall management and execution of Phase I to IV clinical development programs for women's health and andrology. Earlier in her career, Darlene worked at Organon and Knoll Pharmaceuticals in the drug safety and monitoring groups. She has extensive experience in scientific evaluation, implementation and execution of Phase I to IV clinical development programs in a variety of therapeutic areas, with extensive experience in Women's Health and Reproductive Endocrinology. Darlene holds a B.S. in Science and an M.S. in Biology.

Brenda Reese

Tammy Dutkin, Senior Vice President of Clinical Operations

Tammy’s 19 years experience in both pharmaceutical and contract research organizations has given her a depth of experience and insight that translates into successful clinical trials. She began her career performing pre-clinical and laboratory work, and through the years developed an excellent foundation and knowledge base for managing all aspects of drug development from startup to closeout. Prior to joining DSP, she was Vice President at Advanced Clinical Research Services (ACRS) for 11 years. She was instrumental in growing ACRS into a full-service, multi-client biometrics organization, and was responsible for operational management and company strategy. Previously Tammy was Clinical Data Manager at Baxter Healthcare Corporation; and Laboratory Manager at the Chicago College of Pharmacy. Tammy began her career as a research coordinator at the Illinois Institute of Technology Research Institute, where she performed preclinical oncology research. She received her B.S. degree in Biology from Purdue University and her M.S. degree in Psychology from Roosevelt University.

Brenda Reese

Brenda Reese, Vice President of Business Operations

Brenda has worked in the pharmaceutical industry for 15 years, and has extensive experience in clinical research as well as business development. She joined DSP in 2007 as Executive Director of Clinical Monitoring. Brenda’s unique expertise enables DSP to anticipate, understand and solve the challenges sponsors face from both a scientific and business viewpoint. She has a wide depth of experience working within large and small pharmaceuticals companies including Bristol Myers Squibb and Astra Zeneca. Prior to joining DSP, Brenda worked as an Associate Director of Patient Recruitment, and as a Clinical Operations Manager. She has developed and structured two regional monitoring programs within a pharmaceutical company and a contract research organization. Brenda holds a B.S. degree in Nursing and is a registered nurse in the state of California.

Morris Corporate Center 1, 300 Interpace Parkway, Bldg C, Parsippany, NJ 07054 • P: 973-265-1060 F: 973-402-0880