Clinical Trial Associate

Há 2 dias


Lisboa, Portugal TFS HealthScience Tempo inteiro

Overview:
TFS HealthScience is excited to be expanding our
**SRS** team and we are looking for an experienced, highly motivated
**CLINICAL TRIAL ASSOCIATE** who shares our vision of providing clinical research excellence. Our
**SRS **team is a highly experienced international group of professionals led by an industry expert.

We are a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. We combine the full-service capabilities and global reach of a large CRO with the flexibility and personal approach only a mid-size CRO can deliver.

Our cores values of Trust, Quality, Flexibility and Passion are what makes TFS Healthscience the successful company it is today. Our values shape our culture and work ethic. They reflect what we stand for and guide our organisation.

**Together we make a difference.**

TFS HealthScience is looking for a
**CTA** in
** Lisbon**
**.**

As a Clinical Trial Associate, you will be in the Clinical Operations Team and responsible for supporting the Clinical Trial Manager (CTM) and the CMT on operational aspects related to clinical trial conduct to ensure compliance and quality of the clinical trial. You will report to the Senior Director, Team Lead, Trial Management, and work closely with Clinical Operations and other teams and departments.

**What can we offer you?**

A great place to work where you will get the chance to push your career to the next level, global environment with global opportunities. You will also get the opportunity to be part of a team with highly intelligent, passionate experts from all over the world. TFS is a place for inspiration where we focus on the patients, saving lives and aiming to increase their quality of life by supporting our clients.

Health insurance

Hybrid model

Ticket restauran

home alowance

**Responsibilities**:
**Key responsibilities include**:

- Support the Clinical Trial Manager (CTM) and the CMT on operational aspects related to trial conduct to ensure compliance and quality of the trial
- With some guidance, conduct clinical trial support activities related to assigned trials (including coordination and documentation for CTM; critical documentation including sponsor TMF, record management, trial documentation; etc.)
- As directed, provide ongoing support to trials in terms of logistics management, sponsor oversight support, and coordination for outsourcing and contract management
- As required, assist with insurance tracking and coordination as well as budget tool maintenance

Qualifications:

- Bachelor's or Master’s Degree in relevant technical area
- Minimum requirement: 1+ years of experience in clinical trial operations
- Experience with coordination and support activities for clinical trial conduct
- TFS HealthScience collects and processes personal data in accordance with applicable data protection laws. If you are a European Job Applicant see the _
- privacy notice_
- for further details._
- TFS HealthScience does not discriminate on the basis of race, sex, color, religion, age, national origin, marital status, disability, veteran status, genetic information, sexual orientation, gender identity or any other reason prohibited by law in provision of employment opportunities and benefits._



  • Lisboa, Portugal TFS HealthScience Tempo inteiro

    Overview: TFS HealthScience is excited to be expanding our **CTA** team and we are looking for an experienced, highly motivated **CLINICAL TRIAL ASSOCIATE** who shares our vision of providing clinical research excellence. Our **SRS **team is a highly experienced international group of professionals led by an industry expert. We are a leading global...


  • Lisboa, Portugal TFS HealthScience Tempo inteiro

    TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and Functional Service (FSP) solutions. **Join Our Team as a Clinical Trial Associate...


  • Lisboa, Portugal IQVIA Tempo inteiro

    Job Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...


  • Lisboa, Lisboa, Portugal IQVIA Tempo inteiro

    Job OverviewPerform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.Essential FunctionsAssist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...


  • Lisboa, Portugal Novasyte Tempo inteiro

    Clinical Trial Administrator, Single Sponsor dedicated Job Overview: CTA performs daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. By assisting in the coordination and administration of the study activities from the start up...


  • Lisboa, Portugal EPM Scientific Tempo inteiro

    EPM Scientific are currently partnered with a Mid-Sized CRO running a global project in Oncology. They are urgently seeking a Freelance Clinical Research Associate (CRA) to support their expanding clinical operations team. See a short summary below: **Contract Conditions**: - Start date: ASAP - Location: Portugal, Remote - Contract Type: Freelance /...

  • Clinical Trial Specialist

    2 semanas atrás


    Lisboa, Lisboa, Portugal Insight Global Tempo inteiro

    Summary:Participates in electronic QC and indexing of TMF documents as required.Utilizes TMF tools and technology to accomplish tasks without supervision.Proficient in TMF management and can train others.Leads the compilation of the TMF Management Plan and TMF Index in association with the TMF Owner and CROs.Leads the development of TMF technology and tools...


  • Lisboa, Portugal IQVIA Tempo inteiro

    IQVIA is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, Technology, analytics and human ingenuity to drive healthcare forward....


  • Lisboa, Portugal IQVIA Tempo inteiro

    Join us on our exciting journey IQVIA is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, Technology, analytics and human...


  • Lisboa, Portugal Fortrea Tempo inteiro

    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...