Clinical Trials Associate

1 semana atrás

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 (CTA)** 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
**Clinical Trial Associate**
**(**
**Hybrid model**
**)** in
***
**Lisbon**
**.**

**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.

Private Health Coverage

Lunch voucher

**Responsibilities**:

- 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

Moreover, you meet the following personal requirements:

- You are structured and process oriented
- You have a quality mindset and able to prioritize your work in a fast paced and changing environment
- You have good interpersonal and communication skills during interactions with investigators and other external and internal stakeholders
- You can work independently as well as within global teams
- You are result
- and goal-oriented
- 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._

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