Work as a senior data coordinator on clinical and non-clinical trials; producing and validating eCRFs and databases to excellent quality whilst adhering to deliverable timelines. Producing, reviewing and updating eCRF specifications and sections of the Data Handling Manual. Leading clinical coding activities and management of third party data and eCRFs in order to produce a clean database. Acting as lead Data Manager on assigned studies. Working closely with the Sponsor's study team and third party suppliers to meet project deliverables and timelines. Excellent team work ethos, able to manage workload of others, willingness to help others, share skills in a team environment and contribute to process improvement and company profile.

Es posible que un gran número de candidatos se presenten a este puesto, así que asegúrese de enviar su CV y su solicitud lo antes posible.

This role is full-time and fully-remote. The successful candidate may be based in Spain, Poland, France ,South Africa and the UK.

Responsibilities

The following areas of expertise will be aligned to the role...

- Statistical expertise and scientific leadership
- Leadership and people development
- Compliance, quality and governance
- Communication and influence

Qualifications

- Strong English skills, both spoken and written
- Experience of leading studies during database set up, conduct and DBL
- Medidata Rave experience
- Good awareness of clinical trial issues, design, and implementation
- Familiarity with GCP and regulatory requirements




- Experience of data management software systems and some experience of leading data processing activities within a regulated environment
- Experience with Medidata is essential
- Medrio, Viedoc and CrsCube experience is advantageous

Why Join Us

- Remote working and flexible working hours
- Career development, mentorship, and continuous learning
- Supportive, friendly, and collaborative culture

About Phastar

Phastar is an award-winning biometrics and data science CRO, trusted by pharma, biotech, and medical device companies worldwide. With a general team of data specialists, we bring expertise, precision, and pace to every trial, because behind every data point is a patient waiting for treatment.

We transform complex data into clear, actionable intelligence, helping accelerate drug development, and bring life-changing therapies to patients faster.

Awards & Recognition

- SCRIP – Best Contract Research Organization, Specialist Provider
- Citeline – 2025 Award Winner
- Fierce CRO Awards – Recognized Industry Leader

Phastar is committed to the principles and practices of equal opportunities and to encourage the establishment of a diverse workforce. xcskxlj It is our policy to employ individuals on the basis of their suitability for the work to be performed and their potential for development, regardless of age, sex, race, color, nationality, ethnic or national origin, disability, marital status, pregnancy or maternity, sexual orientation, gender reassignment, religion, or belief. This includes creating a culture that fully reflects our commitment to equal opportunities for all.

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📌 Senior Clinical Data Coordinator (España)
🏢 PHASTAR
📍 España