Senior Clinical Specialist

hace 3 semanas


Desde casa, México Signant Health A tiempo completo

(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 create and the services we deliver to our customers.**Where do you fit in?**The Clinical Specialist in the Digital Health Sciences (DHS) team will provide scientific consultation to the commercial and project delivery teams. You will review clinical study protocols from prospective and current customers to identify the scientific and technological requirements of the clinical trial. You will assist in identifying the data collection methods and eCOA solution design based on best practices, patient/site preference, understanding of the therapeutic area, and regulatory guidance. You'll be involved in preparing and attending pre-sales, capabilities, and bid defense presentations and presenting scientific content. Additionally, you'll support the development of eCOA solutions, advising client and internal teams and ensuring clinical trials meet their objectives. You will develop expertise in COA/eCOA across different indications and an understanding of industry trends and advances.*****As part of our team, your main responsibilities will be**:- Support the commercial team by analyzing study protocols and other relevant study documents and documenting study requirements.- Assist in developing client-facing materials and content for strategic and commercial meetings.- Provide guidance on the development of eCOA solutions to client and internal study teams, ensuring the solution design meets study objectives- Understand product capabilities, functionalities, and suitability of solutions across different therapeutic indications.- Maintain comprehensive knowledge of the most recent industry best practices and regulatory requirements for clinical outcome assessments (COA).- Conduct a literature search and review to develop therapeutic area knowledge**Your influence**:Considers all products and services in the context of providing the clinical trial study participant with an optimal participation experience; provides feedback based on practice for potential research areas; participates in patient-centric research efforts. Maintains Signant Health's high regard for scientific expertise and industry leadership.**You’ll need to bring**:- Advanced degree (MSc or Ph.D.) in biological science or related to clinical research.- One to three years of work experience in clinical trial technology or related industry.- Understanding of clinical research and the drug development cycle.- Familiar with the bridge between technology and science in digital health technologies for clinical trials.- Strong interpersonal and communication skills; ability to understand and communicate with stakeholders from a range of disciplines, including clients.- Proven ability to multitask, time management, and task-oriented performance; able to work in a fast-paced environment.- Ability to develop expertise in new fields through research and networking.- Excellent knowledge of spoken and written English.**We’d be thrilled to hear that you also have**:- Advanced degree (MSc or Ph.D.) in Cancer/Oncology or Cardiology/Cardiovascular.- Prior experience in clinical research, preferably in more than one therapeutic area or indication.- Can easily communicate with clients and all levels within the organization.- Prior experience with patient-reported outcome measures (PROs) or Clinical Outcome Assessments (COAs).*****And finally, here are the ways of working that will help you succeed at Signant**:- You enjoy problem-solving and have a constructive can-do attitude.- You’re motivated by working in a fast-growing global company.- You’re self-driven, active, and continuously want to learn new things.- You have excellent communication skills in English, both spoken and written, and can articulate technical details succinctly.- You like to share knowledge as a way to advance organizational learning.**Does this sound like****_something you’d like to explore_****? Then we’d love to hear from you**********Please note that Signant does not accept unsolicited resumes from Third Party vendors.



  • Desde casa, México Parexel A tiempo completo

    **Primary Location**: Mexico, Remote**Additional Locations**: Argentina, Remote; Brazil, Remote**Job ID** R **Category** Clinical Logistics**ABOUT THIS ROLE**:The CSS/Senior CSS has responsibility for the execution of the clinical trial supply logistics strategy on the project.**Key Accountabilities**:**Project Management**- Engaging with Clinical Supply...


  • Desde casa, México IQVIA A tiempo completo

    **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 based upon...


  • Desde casa, México ICON A tiempo completo

    ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations. With our patients at the center of all that we do, we help to accelerate the development...


  • Desde casa, México IQVIA A tiempo completo

    **Job Overview** The Sr. Clinical Data Coordinator performs activities related to the conduct of Phase I - III clinical trials in accordance with ICH/Good Clinical Practices (GCP) and other relevant procedures and guidelines. This role ensures that quality work products are produced, and timelines and deliverables are met. **This position can typically be a...


  • Desde casa, México IQVIA A tiempo completo

    **POSITION TITLE**: Senior Project Manager**REPORTS TO**: Director, Project Management or Designee**BASIC FUNCTIONS**:Responsible for the successful planning, implementation and execution of contracted activities. Assures the accurate transfer of contracts from proposal through project completion. Functionally responsible for all team members throughout the...


  • Desde casa, México Parexel A tiempo completo

    Everything we do has the potential to impact patient lives, and our Clinical Research Associates (CRAs) take their work seriously, demonstrate empathy, and act with heart. They also perform with urgency, navigating our streamlined clinical operating model to drive effectiveness, reduce handoffs and increase employee, client and site satisfaction. As a CRA...


  • Desde casa, México ICON A tiempo completo

    As a Clincial Quality Compliance Lead you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. **What you will be doing**: - Under the leadership of the Operations Quality Lead, develop, contribute, and support facilitation, presentation, and communication of GCP Lessons Learned, GCP...


  • Desde casa, México ICON A tiempo completo

    As Manager Clinical Operations, you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare intelligence.You will be part of an innovative and global Biotechnology company, who pride themselves to be one of the world's leading independent biotechnology companies. They focus on areas with unmet medical...


  • Desde casa, México Parexel A tiempo completo

    Mexico, Remote **Job ID** R0000028052 **Category** Data Management **ABOUT THIS ROLE**: Key Accountabilities: - Data Validation: Lead data cleaning, review, and reconciliation activities. - Documentation: Prepare and maintain DM documents as per SOPs and guidelines. - Study Start-Up: Conduct UAT on clinical database setups and review protocols. Quality...

  • Clinical Data Specialist

    hace 2 semanas


    Desde casa, México IQVIA A tiempo completo

    **Job Overview** Provide basic and some comprehensive data management expertise to the Clinical Data Management (CDM) team to provide efficient, quality data management products that meet customer needs. May also undertake team leadership activities under the supervision of the Data Operations Coordinator (DOC), Data Team Lead (DTL), or Functional Manager....