厚生： Study制度（書籍・講座支援）、Skill研修、リーダーシップ教育、職種別研修、社内公募制度、マッサージルーム、ジム、シャワー室、カフェ、ライブラリー、日替わり弁当無料配布、社内イベント ■勤務時間：フレックスタイム制（コアタイム：11時...
【仕事内容】,名取市小山にある児童発達支援・放課後等デイサービス「HIYOKO STUDY小山教室」♪ ■月給 230,000円～ ■勤務時間 8:00～20:00の間でシフト制実働8時間(休憩60分) ※基本的には8:30...
学校卒に限る ■ 3普通自動車運転免許をお持ちの方 【仕事内容】 仙台市青葉区栗生にある放課後等デイサービス「HIYOKO STUDY栗生教室」♪ ■月給 230,000円〜 ■勤務時間 8:00〜20:00の間でシフト制実働8時間(休憩60...を抱えている子供達の得意なことを伸ばせるよう療育を実施。 さらに、年末年始のお楽しみ会や制作、夏祭りといった多彩なイベントを展開しています。 イベントは、子供が社会的なマナーや協調性を学ぶ良い機会になっていますよ。 ＝生活の基本と自立心を養う＝ HIYOKO STUDY栗生教室では、一人...
success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.... What You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical...
and therapies. What you will be doing Leading the preparation, review, and editing of clinical study documents, including... clinical study protocols, clinical study reports (CSRs), investigator brochures (IBs), and regulatory submissions, ensuring...
working prospect for our people. With numerous wellbeing initiatives, shared parental leave, study assistance and sabbaticals...
with study protocols and regulatory requirements. Collaborating with cross-functional teams to support trial operations... and resolve any issues that arise during the course of the study. Monitoring and tracking trial progress, including managing site...
, and we welcome you to join us on our mission to shape the future of clinical development Job Advert Posting We are currently seeking a Study Start Up Associate... II to join our diverse and dynamic team. As a Study Start Up Associate II at ICON, you will play a pivotal role...
. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study... lifecycle. What You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory...
success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.... What You Will Be Doing: Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical...