Jobs: research associate

**Description**: - Maintain, organize and summarize data associated with multi-locations trials including gathering data before, during and after planting, assisting personnel with field mapping, planting integrated pest management, and other general field activities. - Effectively manage assigned field research activities from experiment planning through...

Our client is a global pharmaceutical company. They are looking for a Clinical Research Associate to join their team. **Responsibilities** - Functioning as project lead for complex BE/Phase I studies and small patient PK/clinical endpoint studies. Serve as liaison between the Mylan project team (Global Pharmacology, Product Development Department Chemistry...

We do Consulting DifferentlyBRG is a global, expert-led consulting firm founded on the principles of entrepreneurialism, collaboration and transparency.  You will join BRG as an Associate/Senior Associate, working on assignments across various industries and moving amongst our core practices, which include: Expert Witness Services in Commercial...

We do Consulting DifferentlyBRG is a global, expert-led consulting firm founded on the principles of entrepreneurialism, collaboration and transparency.  You will join BRG as an Associate/Senior Associate, working on assignments across various industries and moving amongst our core practices, which include: Expert Witness Services in Commercial...

**(Senior) Clinical Research Associate** **Working Model: Thailand** Client Office based/ Bangkok** As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. **What you will be doing**: - Site Monitoring - Site Management - Ultimately reponsible...

As our business grows, we are looking to further strengthen our Clinical Operations team in IQVIA Thailand by hiring Clinical Research Associate (CRA). You will perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and...

As our business grows, we are looking to further strengthen our Clinical Operations team in IQVIA Thailand by hiring Clinical Research Associate (CRA). You will perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and...

Develops strong site relationships and ensures continuity of site relationships through all phases of the trial. Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents. Gains an in-depth understanding of the study protocol...

More than just a recruitment company. At PRTR, we have been a part of our customer's success for 30 years as their total HR solutions partner. With 550 dedicated professionals and over 15,000 outsourced staff, we will continue to carry out our mission to develop a better career, a better life, and a better society, and thrive to become the No.1 people...

As our business grows, we are looking to further strengthen our Clinical Operations team in **IQVIA Thailand** by hiring Clinical Research Associate (CRA). You will perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines,...

**Our Purpose** - Mastercard powers economies and empowers people in 200+ countries and territories worldwide. Together with our customers, we’re helping build a sustainable economy where everyone can prosper. We support a wide range of digital payments choices, making transactions secure, simple, smart and accessible. Our technology and innovation,...

**Are you looking for an exciting next step in your career? Do you enjoy working on high profile global accounts within the FMCG industry?** We are looking for an energetic, self-motivated and passionate individual to join our small but growing team in Bangkok as a Project Administrator. MMR is an independent, global consumer and sensory research agency...

Key Responsibilitiesตรวจสอบและรับรองความถูกต้องของข้อมูลการวิจัยในแหล่งโรงพยาบาล (Source Data Verification - SDV)...

The Manager for Qualitative Research, Consumer Insights assists the Director and Associate Director in leading the qualitative research team and is responsible for supporting the quality of research output as well as the engagement & client management of the practice area. He/she should be recognized and seen as having a strong expertise base in...

Essential Job Duties: - Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits, with or without guidance (as per the training status of the CRAI-MEA); liaise with vendors; and other duties, as assigned - Responsible for aspects...

More about the role:   Senior Associate / Associate are responsible for day-to-day servicing of clients, handling of accounts assigned to them, and initiating and implementing PR activities outlined in a communications program to Burson’s standards.   What you'll do:   Account Management Day-to-day management of allocated accounts according to agreed...

More about the role:   Senior Associate / Associate are responsible for day-to-day servicing of clients, handling of accounts assigned to them, and initiating and implementing PR activities outlined in a communications program to Burson’s standards.   What you'll do:   Account Management Day-to-day management of allocated accounts according to agreed...

**Description** Syneos Health is the only fully integrated biopharmaceutical solutions organization purpose-built to accelerate customer success. We lead with a product development mindset, seamlessly connecting our capabilities to add high-value insights to speed therapies to patients and provide practical value to help our customers achieve their...

Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Essential Functions - Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance...

Develops strong site relationships and ensures continuity of site relationships through all phases of the trial. Performs clinical study site management and monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents. Gains an in-depth understanding of the study...