... will compile, publish and produce Clinical Trial Authorization Applications and associated CTA ... of CTAs The CTA submission manager ensures that key events related to the regulatory aspects of clinical trials are tracked in the company- ...
www.infopraca.pl
... regional demand.Provide data for the ... plan for assessment trials including budget (Trial plan)Organize external (off-station) trials with growers in their crops and internal (in-station) trials with station managers, as planned in the trial planning tool ...
jobs.smartrecruiters.com
... teams, medical experts, and project managers to ensure the highest quality scientific research and statistical analysis. Your Responsibilities: Design and implement statistical strategies for clinical trials within various therapeutic areas. Develop ...
pl.talent.com
... outcomes, enhance clinical practice and support business needs at the national, regional and corporate levelbr * Demonstrate the ... , congress materials, clinical trials and real-world databr * Ensure ... with the Manager, and liaises with the other ...
www.iagora.com
... a highly experienced and motivated Clinical Trials Lead Programmer to join our ... programming technology and techniques, clinical trials, and developments in the pharmaceutical ... at least 6 years of clinical trial experience as a statistical programmer ...
pl.talent.com
... teams, medical experts, and project managers to ensure the highest quality scientific research and statistical analysis. Your Responsibilities: Design and implement statistical strategies for clinical trials within various therapeutic areas. Develop ...
pl.jooble.org
... a highly experienced and motivated Clinical Trials Lead Programmer to join our ... programming technology and techniques, clinical trials, and developments in the pharmaceutical ... at least 6 years of clinical trial experience as a statistical programmer ...
pl.jooble.org
... very heart of every successful clinical trial. Working alongside brilliant minds across ...
pl.talent.com
... members of the group : * For clinical trial protocols under the ownership of ... of the protocol. o For clinical trial protocols under the ownership of ...
www.iagora.com
... working with the physicians within Clinical Development to provide clinical research support for programs as ... at least 5 years as clinical research scientist in oncology are ... ,000 Sites and 675,000+ Trial patients. No matter what your ...
pl.jooble.org