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Medical Science Liaison/Sr. Clinical Research Associates

If you believe SECC might be of assistance to you for a single staff member or with our entire team

SWAT

“SWAT” is a term we use to describe how our clinical and data experts are brought in to quickly resolve these serious problems and restore your confidence in the study. We have often been called upon to resolved matters which study managers (sponsor) notes deficient issues relative to data review, site supervision and or visit consistency. We can help. Our services involve an intense work ethic, the use of our expert, experienced and specialized monitors, data managers and regulatory experts.

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Benefits of Medical Science Liaison

They also play a role in our corporate service development to our clients

WHO ARE THEY?

SECC MSLs come from a variety of backgrounds, for example, pharmacy, academia and clinical research. Each contributes unique perspectives. MSLs are selected as much on the basis of their personal and professional qualities as for their experience: honesty and integrity; innovation and creativity; dedication to excellence; a sense of urgency; and excellent interpersonal and administrative skills.

WHY ARE THEY NECESSARY?

To meet licensing requirements, clinical trials of new therapeutic agents must focus on FDA-defined primary endpoints. But these studies may fail to address or yield incomplete information on other key clinical questions - such as rejection incidence, optimal dosing, efficacy and safety in combination with other new agents, drug interactions, and potential for use in other patient types or indications. Physicians working daily in the fields know what factors are crucial in deriving the greatest benefit from a new therapy. That's where MSLs come in, interacting with investigators to fund, develop, implement and manage research into these interesting and important clinical issues.

WHAT DO THEY DO?

MSLs play a significant role in SECC clinical research projects - usually Phase IV trials of products that have been cleared for marketing FDA. They may do any or all of the following:

  • Manage study contracts, Payments and grants
  • Assist in protocol and forms development
  • Ensure timely availability of study supplies
  • Assist in study initiation, patient enrollment, management, monitoring, data collection and analysis
  • Liaise with CRO's study sites and sponsors
  • Facilitate study reporting and publication
  • ORGANIZED FOR ACTION

    MSL activities are integrated and coordinated at two levels. The group itself is formed into several Field Project Teams, each responsible for all MSL activities within one of the following therapeutic areas:

  • Oncology
  • Cardiology
  • Infectious diseases
  • Rheumatology
  • Autoimmune diseases
  • OUR THERAPEUTIC EXPERIENCE

  • Neurology
  • Urology
  • Cardiology
  • Oncology
  • Infectious Disease
  • CNS
  • Men Health
  • Women's Health
  • Cardiac - Device
  • Urology Device
  • Vaccine
  • Gastroenterology
  • Pain Management
  • and many more...
  • CONTINUING EDUCATION SERVICES

    MSLs review the current medical literature and attend medical and other relevant meetings to maintain and expand their professional knowledge. You can count on their capacity to understand and help. Extensive Knowledge of clinical therapeutic in their assigned areas equips them to perform valuable educational services, such as staff training, presentation of research data, and in-services. them. With its commitment to quality services and qualified, experienced consultants, SECC I is the premier choice for pharmaceutical and biotechnology companies in need of expert clinical monitoring, project management, and educational services. Other services available through SECC upon request include; auditing, medical writing, protocol development, and Case Report Form design.

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