Clinical Trial Reg Affairs Snr Assistant

**IQVIA Biotech is committed and dedicated to the small biotech & biopharma companies we support.** **Opportunities available for an experienced Clinical Trial Manager II or Senior Clinical Trial Manager.** **Previous clinical trial management and CRO experience preferred.** **Therapeutic **requirements/preference**: any of the following...

Internal Job Description - ** Experience managing clinical trials in LATAM and North America(REQUIRED)**: - ** Strong Cardiovascular Therapeutic experience**: - **3+ years of Clinical Trial Management experience (CRO experience preferred)** **BASIC FUNCTIONS**: Responsible for the successful planning, implementation and execution of contracted clinical...

**It takes curiosity and intellectual courage to accomplish great things. It takes brave minds to bring powerful ideas to reality and transform healthcare. We are a diverse, global team that shares a passion for collaboration and solving complex problems. Together, we help customers drive healthcare forward.**: **Join IQVIA and see where your skills can take...

As part of Parexel Consulting, you will create and maximize value for clients throughout the product lifecycle. You will be a strategic guide in getting products to market faster, smarter - and keeping them there -your scientific, technical, regulatory, and/or commercial expertise will put best practice standards to work for biopharmaceutical and medical...

Act as an administrator for our in-house Regulatory Intelligence database and provide customer support for issues arising. - Regulatory collaboration with Regulatory Intelligence database workflow users to drive quarterly EQR metrics. - Contribute to a wide range of technical Regulatory Intelligence database content projects including engineering and...

**POSITION TITLE**: Regulatory Affairs Specialist **REPORTS TO**: Manager, Regulatory Affairs or Designee **BASIC FUNCTIONS**: **ESSENTIAL JOB FUNCTIONS, DUTIES AND RESPONSIBILITIES**: - Assist Manager, Regulatory Affairs, in assuming primary or secondary regulatory responsibility for assigned clinical research projects by providing regulatory...

(This is a remote role located in Mexico) *** **Want to do the Best Work of Your Life?** Working at Signant Health puts you at the very heart of the world’s most exciting sector - a high-growth, dynamic company in an extraordinary industry. We’re radically changing the clinical trial landscape, driving change through the technology and innovations we...

We are a growing stuffing agency that creates the connection between Managers who want to organize their life and to improve their life quality and Executive assistants who help the managers to reach their goals. We give the business owners and founders from the US and Western Europe the FREEDOM and time to focus on more important tasks. With our service an...

Supports the preparation of documentation and submissions under guidance - Coordinates and manages client deliverables supporting regulatory compliance - Liaises with internal and external clients in the tracking and status update of project plans and overall support of projects - Assists with project budgeting/forecasting - Maintains knowledge and...

**POSITION TITLE**: Senior Clinical Data Specialist **REPORTS TO**: Associate Manager/Manager, Data Management or Designee **BASIC FUNCTIONS**: **ESSENTIAL JOB FUNCTIONS, DUTIES AND RESPONSIBILITIES**: - Clinical Data and Query Review: - Create listings using ad hoc query tools - Issue queries and review query responses with the highest level of quality...

**POSITION TITLE**: Senior Clinical Data Specialist **REPORTS TO**: Associate Manager/Manager, Data Management or Designee **BASIC FUNCTIONS**: **ESSENTIAL JOB FUNCTIONS, DUTIES AND RESPONSIBILITIES**: - Clinical Data and Query Review: - Create listings using ad hoc query tools - Issue queries and review query responses with the highest level of quality...

Investigator Relationship Specialist (Clinical Trials) Summary: **Responsibilities**: - Contact doctors and medical professionals to introduce them to our clinical trials. - Build and maintain relationships with medical professionals to facilitate enrollment in clinical trials. - Provide information and answer questions about clinical trials to medical...

Mexico, Remote **Job ID** R0000013690 **Category** Clinical Logistics **ABOUT THIS ROLE**: The CSS has responsibility for the execution of the clinical trial supply logistics strategy on the project. **Skills** - Client focused approach to work - Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to...

**Job Overview** Manage a team of clinical staff working in support of clinical studies to ensure projects are appropriately resourced and employees are trained and meeting project objectives. **Essential Functions** - Manage staff in accordance with organization’s policies and applicable regulations. Responsibilities include planning, assigning, and...

Project Support Coordinator Completes a wide variety of technical, logístical, facilitative and central processes that are critical to study success; Provides project administrative support, including planning, organizing and coordinating responsibilities for Project Leads, Clinical Team Managers and other functional leads on designated projects throughout...

Job Overview Perform monitoring and site management work for a variety of protocols, site and therapeutic areas. Essential Functions - Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference...

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...

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...

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...

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...