Arama sonuçları: 10 ilan
...excellence, and we welcome you to join us on our mission to shape the future of clinical development.
What you will be doing:
As a Sr CTA you will be working closely with the wider project team to support the management of investigative sites and ensure that all sites...
...excellence, and we welcome you to join us on our mission to shape the future of clinical development.
What you will be doing:
As a Sr CTA you will be working closely with the wider project team to support the management of investigative sites and ensure that all sites...
Uzaktan çalışma
...CTA (Junior) - Based in Istanbul
FSP - Sponsor Dedicated
Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes...
...We are looking for a (Senior) Regulatory Affairs Associate with Clinical Trial Submissions (CTA) experience to join our growing team in Istanbul.
This role is office based in Turkey (hybrid model is also available).
As a Senior Regulatory Affairs Associate you will...
...confidentiality
• Other duties as assigned
You will need:
• Minimum Bachelor's degree in a life science
• At least 12 months of a CTA/Clinical Trial Coordinator or similar role experience within the clinical/pharmaceutical industry
• Understanding of ICH GCP...
...pre-trial assessment, subject recruitment and retention planning, site initiation, monitoring and close-out.
Partnering with the CTA, LTM and GTM to ensure overall site management while performing trial related activities for assigned protocols.
May contribute to...
...At least two years of proven managerial experience;
At least two years of clinical trials related experience (as investigator, CTA, IHCRA etc.);
Complete understanding of and experience in delivering in line with ICH GCP Compliance;
Excellent communication and...
...qualification in nursing, life sciences or medical sciences;
At least two years of clinical trials related experience (as investigator, CTA, IHCRA etc.);
Minimum one year of experience in oncology protocols;
Profound understanding of ICH GCP Compliance;
Ability to...
...through coordination with state govt. / local municipal bodies / State or District Broadband Committees.
b. Acquisition support for CTA & Government sites aligned with gazette notification on RoW
# Knowledge Certifications and Experience...
...completed on time, including preparation of IRB/IEC submission packages, review of Informed Consent Forms, engaging Regulatory Affairs/CTA Hub for Health Authorities submissions, as required
• Prepares and finalizes local submission package for submission to IRB/IEC,...