PSI CRO

More roles at PSI CRO

Senior Clinical Research Associate

Work from home

Remote role where the employee must remain based in a particular country.

Netherlands only

From the employer's advert: Independent on-site monitoring experience in the Netherlands

Employer listed it 4 weeks ago · Added 4 weeks ago

Been open since 4 weeks ago, still being checked, but it has been live a while.

Salary

Not stated

Location

Netherlands only

Timezone

CET ±2

Contract

Full-time

Experience

Senior

What the advert says

Quoted word for word from the employer's advert. Where it says nothing, we say so.

Working hours: Not mentioned in the advert
Where you can work from: Conducting and reporting all types of onsite monitoring visits
Contract: Not mentioned in the advert
Experience asked for: Not mentioned in the advert
Pay: Not mentioned in the advert

Remote flexibility

Work from home

This is a remote role, but the employee must be based in Netherlands. It is work from home rather than work from anywhere.

What the employer says

Source listing states candidate location: "Utrecht, UT, Netherlands, Utrecht, UT, nl, Remote"

What Nomaders makes of it

Residency required in Netherlands
Payroll and tax are likely handled in that country only

The quotes above are the employer's own words; the reading is ours. Always check the original listing and employment terms before working from another country.

Before you apply

Experience: employer states

Written as a requirement

“Experience supporting Oncology studies is beneficial, but not essential”

Questions worth asking: Nomaders interpretation

No pay is stated. Ask for the salary range before investing time in interviews.
The advert does not say whether this is employment or a contractor arrangement. Ask, as it affects tax and benefits.

Produced automatically from this advert's text; not reviewed by a person. The employer's own page is the final word.

About the role

PSI is a leading Contract Research Organisation with 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.

As a Senior CRA, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. Your focus will be on subjects’ rights, safety and well-being and quality of data compliance.

This is a home-based position. 

Your responsibilities will include:

Conducting and reporting all types of onsite monitoring visits

Driving the study startup phase 

Performing CRF reviews, source document verification and query resolution

Be responsible for site communication and management

Supervising study activities, timelines, and schedules for each site

Acting as a point of contact for in-house support services and vendors

Supporting quality control, such as compliance monitoring and reports review

Participating in feasibility research

Supporting the regulatory team in preparing documents for study submissions and regulatory approval

BSc or MSc in Life Sciences (or similar), or an equivalent combination of education, training & experience

Independent on-site monitoring experience in the Netherlands

Demonstrable experience in all types of monitoring visits in Phase II and/or III

Strong written and verbal communication skills

Fluency in Dutch and English

Experience supporting Oncology studies is beneficial, but not essential

Advanced knowledge of MS Office

Full and clean driver's license, and the ability to travel

Communication, collaboration, and problem-solving skills are essential

Ability to multitask and work in a dynamic team environment

Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.

Requirements

·Fluency in Dutch and English
·Experience supporting Oncology studies is beneficial, but not essential
·Advanced knowledge of MS Office
·Full and clean driver's license, and the ability to travel
·Communication, collaboration, and problem-solving skills are essential

Benefits

No benefits package published with this listing. Ask about it at first interview.

How to apply

1Check the flexibility label above, work from home, matches where you plan to live and work.
2Tailor your CV to the role at PSI CRO, mentioning your remote working experience and working hours (CET ±2).
3Apply directly on the employer's careers page using the button below. Nomaders never handles your application.

Found 27d ago. Last checked today. Always confirm the details on the original posting, salary and location can change after publication.

Listing sourced from Company boards.