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Contract Specialist



Introductie

The organisation is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services.

Het bedrijf / The company

The organisation is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. They provides services for pharmaceutical, biotechnology, medical device, academic and government organizations. Also open for junior candidates.

De functie / The role

In this role you will draft, review and negotiate agreements with clinical study sites and principal investigators ("Clinical Trial Agreements" (CTA)). Serve as the primary contact for all Clinical Trial Agreements for all clinical studies assigned to your group and must be able to work independently, while consulting with Company attorneys and other key individuals as appropriate and necessary. Draft and review CTA and associated contracts related to CTAs according to Company policy, rules, practices and procedures and implement and manage the process for internal and external approval, execution and filing of CTAs and associated contracts. Identify and assist with the implementation of process improvement opportunities. Maintain contact and relationships with all internal departments, Senior Management and clients and shall identify and protect the company and its clients from unnecessary business and legal risk.

Het profiel / Your profile

Qualifications for the function as a Contract Specialist:

Educated at degree level;
Significant experience in contract drafting and negotiation experience;
Or equivalent combination of education and experience that provides the knowledge, skills, and abilities to perform the job.
Knowledge, Skills and Abilities:

Excellent communication and interpersonal skills;
Excellent organizational skills and strong attention to detail with proven ability to handle multiple tasks efficiently and effectively;
Flexible and able to reprioritize workload to meet changing project needs;
Excellent MS Excel and MS Word skills;
Excellent English,Dutch and grammar skills;
Excellent analytical and decision based thinking;
Capable, with appropriate oversight, of drafting and negotiating contract provisions;
Must be able to work independently and as a team player;
Must be able to provide direction to other employees;
Responsible for understanding and adhering to the SOPs, WPDs and other regulations for all aspects of project implementation, execution and closeout.

Reactie / Reaction

More information about the contract specialist? Please contact Leonie Koomen at Leonie@heraklespharma.nl or 06-1051 83 23


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.


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Gegevens

Werkgever:
Anoniem
Vacaturesteller:
Herakles
Standplaats:
Utrecht

Geplaatst op FMF: 04 januari 2019

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