Senior Clinical Research Associate

**Job Description**: We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we “follow the science” that great medicines can make a significant impact to our world. We believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that...

The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager or CRD, the person ensures compliance of study conduct with ICH/GCP and country regulations, Company policies and procedures, quality standards and adverse event reporting requirements internally and externally. Acts as...

The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the Clinical Research Associate manager the person ensures compliance of study conduct with International Conference on Harmonisation Good Clinical Practice and country regulations, our company policies and procedures, quality...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager or CRD, the person ensures compliance of study conduct with ICH/GCP and country regulations, Merck/MSD policies and procedures, quality standards and adverse event reporting requirements internally and externally. Acts...

**Job Description**: The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country regulations, Merck/MSD policies and procedures, quality standards and adverse event reporting requirements internally and...

**Job Description**: The role is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the Clinical Research Associate manager the person ensures compliance of study conduct with International Conference on Harmonisation Good Clinical Practice and country regulations, our company policies and...

The Clinical Research Associate II (CRA II) is responsible and accountable for site monitoring and site management. Has responsibility for clinical studies according to Company, and/or Sponsor Standard Operating Procedures, and local regulatory guidelines. Assures the implementation of project plans, as assigned. Act in the project role of a Local Project...

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...

Company Description We are the company that cares - for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,500 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those...

Great opportunity if you want to join one of the greatest CROs! Job Overview Perform a variety of administrative tasks in support of clinical trials and assist in the performance of clinical procedures to collect data on patients enrolled and/or seeking enrollment in clinical studies. Essential Functions - Provide clinical research support to...

Company Description PSI is a leading Contract Research Organization with more than 25 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. **Job Description**: Join our international team and be the...

Join our team as an **Evidence Synthesis Associate Consultant** supporting rigorous analyses and critical appraisals of published medical evidence across a wide range of diagnostic, prognostic, therapeutic, and other clinical interventions, as well as drafting reports. This professional will also provide technical expertise on evidence synthesis methods,...

**HOW MIGHT YOU DEFY IMAGINATION?** If you feel like you’re part of something bigger, it’s because you are. At Amgen, our shared mission—to serve patients—drives all that we do. It is key to our becoming one of the world’s leading biotechnology companies. We are global collaborators who achieve together—researching, manufacturing, and delivering...

Company Description PSI is a leading Contract Research Organization with more than 25 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. **Job Description**: Join our international team and be the...

Manage the daily operational activities in Puerto Rico of GPRD Phase I to IV clinical studies monitored by Abbvie in accordance with GCP/ICH guidelines and AbbVie SOPs. - Ensures clinical trial activities are conducted according to the monitoring plan and are in accordance with project timeliness and company objectives. Anticipates and identifies site issues...

We are recruiting a **Research Associate** who has experience and relevant training in conducting quantitative and/or qualitative research to work on projects supporting just transitions and economic diversification beyond fossil fuel extraction in Latin American countries. **Location**:Bogota, Latin America **Type of contract**: Full-time, fixed-term...

Job Overview Provide centralized task support on all assigned projects. Ensure all work is conducted in accordance with SOPs, work instructions, policies, good clinical practices and applicable regulatory requirements. Comply with all associated quality and timeliness metrics. Essential Functions - Liaise with project teams and third party vendors to...

Job Overview Acts as Lead Programmer to plan and coordinate database design, development, implementation, maintenance, and user support of clinical systems. Provides technical expertise in conjunction with domain knowledge to create programs using statistical analysis system language to support client clinical data studies Essential Functions - Acts as...

**Job Information**: Work Arrangement **Onsite** *** City **Bogota** *** State/Province **Distrito Capital de Bogotá** *** Country **Colombia** *** **Fuel Your Future and Redefine Hospitality!** Fuel your future as a Senior Associate in Real Estate Partnerships, where teamwork makes the dream work. Embrace a work-life balance that aligns with our...