TRABAJO PRINCIPAL INVESTIGATOR

Strong decision maker capable of simultaneously working on and in several fast-paced projects... preference will be given to candidates with experience in translational...

As we expand our clinical/regulatory department, we are actively seeking a talented and experienced principal regulatory writer to join our team... key responsibilities:regulatory...

  as principal medical writer, you will be supporting a top-5 biotech company... as a principal medical writer you will be joining the world’s largest...

Authoring experience with investigator brochures, clinical study protocols, and clinical study reports... within integrated data analytics & reporting (idar)...

€¢ supports responses to regulatory questions on the design of the program, and any labelling claims following submission • participates in presentations at client...

Summary the principal statistician supports the design, execution, analysis, interpretation, and reporting or communication of data evidence for pre/early/late clinical...

Within integrated data analytics & reporting (idar), the regulatory medical writing team are recruiting for a  principal medical writing scientist  ...

Com within integrated data analytics & reporting (idar), the regulatory medical writing team are recruiting for a principal medical writing scientist to support...

Fundraising (international): projects obtained from international funding sources as principal investigator/coordinator in the previous 5 years (i...

) outside parties external: • clinical investigator sites • commercial suppliers • clinical research organizations (when applicable)... ensure familiarity with departmental...

Applications should include the following documents (in pdf format): written support of the principal investigator of the in host lab...   how to apply before submitting...

Attends/participates in investigator meetings as needed... may schedule and conduct a local/country investigator meeting conducts local trial team meetings and provides...

Attends/participates in investigator meetings as needed... qualifications ＜職務経験＞ ・治験実務あるいはモニタリング業務経験　5年以上 ・国内臨床試験および国際共同試験の施設選定からデーターベースロックまでのモニタリング経験 ・治験の実務を通じた後輩社員の指導...

Liaising between research group leaders and other iciq support areas for the daily running of the projects project coordination: monitor the progress of work, anticipate...

principal responsibilities: 1... attends/participates in investigator meetings as needed... principal relationships: primary reporting structure: reports to a functional...

Attends/participates in investigator meetings as needed... principal responsibilities: (list major responsibilities and duties of the position...

Partner with academic research team on investigator sponsored studies... principal duties and responsibilities: work in matrix partnerships with chief medical officer...

Day to day responsibilities will include: support clinical research studies and maintain a safe study environment according to health and safety policies under the...

Day to day responsibilities will include: support clinical research studies and maintain a safe study environment according to health and safety policies under...