home
vacatures
job-alert
bemiddelaars en links
over FMF
FAQ
vacature plaatsen
tell a friend
Tell a
Friend


Vacature ingevuld? Meld het ons!
Vacature
vervuld?



Opgeslagen
vacatures (0)
Solliciteer hier
Indien solliciteer hier u verwijst naar een ongeldig webadres, is de vacature (hoogstwaarschijnlijk) inmiddels vervuld. Attendeer FMF hierop
favvacicon

CRA (mrt ervaring)



Introductie

The Clinical Research Associate (CRA) performs and coordinates all aspects of the clinical monitoring and site management process in accordance with ICH Good Clinical Practices, FDA guidelines, local regulations and Standard Operating Procedures.

De functie / The role


Conducts site visits to assess protocol and regulatory compliance and manages required documentation.
Responsible for ensuring that data will pass international quality assurance audits.
Represents the company in the global medical research community and develops and maintains collaborative relationships with investigational sites and client company personnel.
Will assist project manager or clinical team manager on assigned projects and will take a lead role where required.
Will support the line manager to mentor, train and contribute to the development of junior clinical team members.
Required to travel 60% on average.

Het profiel / Your profile

Functie eisen
Education and Experience:

University degree in a science related field or a certified health care professional or equivalent certification/licensure from an appropriately accredited institution
Considerable clinical research monitoring experience (comparable to 5 years) with a demonstrated high level of expertise in all aspects of clinical monitoring
Fluency in English and in the country's native language
Valid Driver's License where applicable
In some cases an equivalent combination of education, professional training, and experience that provides the required Knowledge, Skills and Abilities may be considered
Knowledge, Skills and Abilities:

Expert clinical monitoring skills
Expert knowledge of FDA guidelines, GCPs and applicable Standard Operating Procedures
Skills to mentor and train other monitors in a positive and effective manner
Demonstrated ability to evaluate medical research data and proficient knowledge of medical terminology
Excellent oral and written communication skills
Strong customer focus
Excellent interpersonal skills
Excellent organizational and time management skills
Strong attention to detail
Proven flexibility and adaptability
Excellent team player with team building skills
Effective presentation skills
Ability to work independently as required
Ability to utilize problem-solving techniques applicable to constantly changing environment
Good computer skills: good knowledge of Microsoft Office and the ability to learn appropriate software

Reactie / Reaction

Contactpersoon
Sacha Goossens
T: (020) 3118 770
E: s.goossens@farmasel.nl


Solliciteer hier
Indien solliciteer hier u verwijst naar een ongeldig webadres, is de vacature (hoogstwaarschijnlijk) inmiddels vervuld. Attendeer FMF hierop

Uw referentie aan www.fmfvacatures.nl wordt gewaardeerd.
Your referral to www.fmfvacatures.nl is appreciated.


tussenpersoonlogo

Gegevens

Werkgever:
Anoniem
Vacaturesteller:
Farmasel
Standplaats:
Nederland

Geplaatst op FMF: 14 maart 2019

Branche: Farma & Biotech
Functie: Clinical research
Opleidingsniveau: WO/academisch / MSc
Werkervaring: 2-5 jaar, 5-10 jaar, > 10 jaar