1040 English-speaking jobs in Occitania

Job Purpose To implement project management of clinical trials effectively, and to ensure success of clinical trials. 2. Responsibilities Make the project management plan: To draft and implement feasible project management plan according to SOPs , ICH GCP Guidelines, ISO14155 and other applicable regulations. Ensure the trial in managed under the project management plan.

Job Purpose To implement project management of clinical trials effectively, and to ensure success of clinical trials. 2. Responsibilities Make the project management plan: To draft and implement feasible project management plan according to SOPs , ICH GCP Guidelines, ISO14155 and other applicable regulations. Ensure the trial in managed under the project management plan.

Job Purpose This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical studies in accordance with Tigermed Jyton or sponsor Standard Operating Procedures (SOPs), International Conference on Harmonization Good Clinical Practice standard (GCP), ISO14155 and other applicable regulations.

Job Purpose To implement project management of clinical trials effectively, and to ensure success of clinical trials. 2. Responsibilities Make the project management plan: To draft and implement feasible project management plan according to SOPs , ICH GCP Guidelines, ISO14155 and other applicable regulations. Ensure the trial in managed under the project management plan.

Job Purpose This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical studies in accordance with Tigermed Jyton or sponsor Standard Operating Procedures (SOPs), International Conference on Harmonization Good Clinical Practice standard (GCP), ISO14155 and other applicable regulations.

Job Purpose To implement project management of clinical trials effectively, and to ensure success of clinical trials. 2. Responsibilities Make the project management plan: To draft and implement feasible project management plan according to SOPs , ICH GCP Guidelines, ISO14155 and other applicable regulations. Ensure the trial in managed under the project management plan.

Clinical Research Associate II – Paris (Home-Based) Chloe O'Shea has partnered with a large global CRO renowned for delivering innovative, high-quality solutions in clinical development. We are seeking an experienced Clinical Research Associate II (CRA II) to join a dedicated single-sponsor team in Paris.

Clinical Research Associate II – Paris (Home-Based) Chloe O'Shea has partnered with a large global CRO renowned for delivering innovative, high-quality solutions in clinical development. We are seeking an experienced Clinical Research Associate II (CRA II) to join a dedicated single-sponsor team in Paris.

Clinical Research Associate II – Paris (Home-Based) Chloe O'Shea has partnered with a large global CRO renowned for delivering innovative, high-quality solutions in clinical development. We are seeking an experienced Clinical Research Associate II (CRA II) to join a dedicated single-sponsor team in Paris.

Clinical Research Associate II – Paris (Home-Based) Chloe O'Shea has partnered with a large global CRO renowned for delivering innovative, high-quality solutions in clinical development. We are seeking an experienced Clinical Research Associate II (CRA II) to join a dedicated single-sponsor team in Paris.

Clinical Research Associate II – Paris (Home-Based) Chloe O'Shea has partnered with a large global CRO renowned for delivering innovative, high-quality solutions in clinical development. We are seeking an experienced Clinical Research Associate II (CRA II) to join a dedicated single-sponsor team in Paris.

Clinical Research Associate II – Paris (Home-Based) Chloe O'Shea has partnered with a large global CRO renowned for delivering innovative, high-quality solutions in clinical development. We are seeking an experienced Clinical Research Associate II (CRA II) to join a dedicated single-sponsor team in Paris.

Clinical Research Associate II – Paris (Home-Based) Chloe O'Shea has partnered with a large global CRO renowned for delivering innovative, high-quality solutions in clinical development. We are seeking an experienced Clinical Research Associate II (CRA II) to join a dedicated single-sponsor team in Paris.

Clinical Research Associate II – Paris (Home-Based) Chloe O'Shea has partnered with a large global CRO renowned for delivering innovative, high-quality solutions in clinical development. We are seeking an experienced Clinical Research Associate II (CRA II) to join a dedicated single-sponsor team in Paris.

Head of New Product Development (NPD) Location: Nationwide (Remote – with up to 50% international travel) Language: Fluency in English is essential for collaboration across our global teams.

Head of New Product Development (NPD) Location: Nationwide (Remote – with up to 50% international travel) Language: Fluency in English is essential for collaboration across our global teams.

Head of New Product Development (NPD) Location: Nationwide (Remote – with up to 50% international travel) Language: Fluency in English is essential for collaboration across our global teams.

Head of New Product Development (NPD) Location: Nationwide (Remote – with up to 50% international travel) Language: Fluency in English is essential for collaboration across our global teams.

Head of New Product Development (NPD) Location: Nationwide (Remote – with up to 50% international travel) Language: Fluency in English is essential for collaboration across our global teams.

Head of New Product Development (NPD) Location: Nationwide (Remote – with up to 50% international travel) Language: Fluency in English is essential for collaboration across our global teams.