Position Summary: (Briefly state the objectives of this position) A Site Manager II (SM II) serves as the primary contact point between the Sponsor and the Investigational Site. A Site Manager II is assigned to trial
1. Principal Duties and Responsibilities (General Summary , essential functions and authorities, etc.) 主要工作职责(基本概况,主要功能,权限等) General Summary(基本概况) Increase product, treatment awareness and technique perception through elevated awareness and improvements in clinical research/ observations, publications and data management, strategically provide channel
Position Summary: (Briefly state the objectives of this position) The Local Trial Manager II (LTM II) is responsible for local management of a clinical trial (or Medical Affairs data generation activity) in a country or countries. The LTM II
Position Summary: (Briefly state the objectives of this position) A Site Manager serves as the primary contact point between the Sponsor and the Investigational Site. A Site Manager is assigned to trial sites to ensure inspection
POSITION SUMMARY : Briefly state the objective of this position. Why the job exists (2-3 sentence maximum) • Lead MSL team for KOL engagement and regional medical activities • Cooperate with MA team and sales team
Overview of MAF Function and the TA Head role The TA Head is responsible for leading the medical team of Medical Advisors, MSLs & Medical Education teams to formulate medical strategy that is aligned to the
POSITION SUMMARY : Briefly state the objective of this position. Why the job exists (2-3 sentence maximum) • Contribution to ME strategy development in the relevant therapeutic area and product. • Communicate with cross-function to make
Position Summary: (Briefly state the objectives of this position) A Site Manager II (SM II) serves as the primary contact point between the Sponsor and the Investigational Site. A Site Manager II is assigned to trial
Job Description: Overall purpose of job: • Develop and implement market access strategies and tactics to maximize the access of our stakeholders to our products. • Manage the coordination of regulatory submission between regulatory affairs, new
Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world
Description Kenvue is currently recruiting for: Senior Programmer Who We Are At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, were the house of
Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world
Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world
Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world
Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world
Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world
Job Description Summarized Purpose: Performs and coordinates all aspects of the clinical monitoring and site management process in accordance with ICH GCP, FDA guidelines, local regulations and PPD SOPs. Conducts site visits to assess protocol and regulatory compliance
Job Description At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world
Job Description Are you ready for an amazing opportunity that truly will make a difference, with an amazing team and incredible leadership? If so, you are in the right place! We are vital links between an
Job Description • Manages all clinical operational and quality aspects of allocated studies, of low to moderate complexity, in compliance with ICH GCP. • Develops clinical tools (e.g. Monitoring Plan, Monitoring Guidelines) in conjunction with the Data Quality Plan.