Study Coordinator

hace 12 horas

Madrid, España TFS HealthScience A tiempo completo

Overview:
TFS HealthScience is excited to be expanding our SRS
** **team and we are looking for an experienced, highly motivated Study Coordinator 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 Study Coordinator in Madrid

This role will sit embedded within one of our prestigious clients who promotes rapid career development

**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.

**Benefits include**:
Lunch allowance

Health Insurance

Flexible working times

Home allowance

Flexible remuneration

**Responsibilities**:
The Site Coordinator is part of the Site Coordinators Unit within Medical Affairs Organization and will work operationally as a member of the Study Team at the investigational site.

The Site Coordinator works to facilitate the Principal Investigator (PI) job, contribute to the quality in the study, give appropriate support to reach the milestones, pro-active recruit new patients and reduce data-entry times.

Work is conducted according to company policies, SOPs and regulatory requirements.

Responsibilities:

- Data Entry
- Queries resolution
- Assist with SAE notification
- Help investigator with patient recruitment
- Facilitate Ethics Committee submissions
- Attend Monitoring visits
- Investigator File updating
- Patient visits schedule
- Study Drug Accountability and Dispensing logs
- Sample shipment
- Patients expenses payment
- Assist in investigators meetings or training when required

Position Requirements

Qualifications:
Bachelor’s Degree in life science

Excellent organizational skills and demonstrated ability to prioritize and handle multiple

competing priorities

Adaptability and flexibility to changing priorities, with ability to maintain demanding timelines

Good oral, written and communication skills in English

Ability and willingness to travel
- 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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