CLINICAL TRIAL MANAGER (part-time) Ref.: CTM/ST

COMPANY

Pharmaceutical services

We are looking for an organized Clinical Trial Manager to implement and oversee projects, and to ensure quality of trials.

The Clinical Trial Manager collaborates with the Clinical Project Manager to review budgets, make changes where necessary, and outline project together with client and clinical monitoring team.

The Clinical Trial Manager regularly visits Clinical Trial Investigators, issues them supplies, such as Case Report Forms and Investigational Product, and oversees Clinical Research Associate travel expenses and time sheets. You will gather Case Report Forms and ascertain their quality, and collaborate with Clinical Trial Investigators to write final technical reports.

To be successful in this role you need to ensure the project meets the client's goals within budget and on time.

Top candidates are proficient multitaskers, client-oriented and have the ability to prioritize tasks.

 

 

Responsibilities:

 

  • Collaborating with Project Manager to set targets for clinical monitoring staff, and ensuring recording of trial in compliance with project goals.

  • Creating and implementing study-specific clinical monitoring tools and documents.

  • Creating and overseeing trial budget.

  • Identifying, enlisting and choosing sites, and coordinating site management activities.

  • Coordinating and supervising clinical monitoring team.

  • Providing Clinical Research Associates with project-specific training and having regular meetings with them.

  • Recording and sharing interactions with client, and acting as their representative.

  • Arranging and overseeing site visits.

  • Gathering and examining trial documents.

  • Assuring compliance SOPs and local regulations, and CFR, ICH and GCP guidelines.

Requirements:

  • Bachelor’s degree in medicine, science or equivalent degree/experience.

  • 3+ years work experience in diabetological area for pharmaceutical company.

  • Proficient understanding of marketing and statistics.

  • Outstanding communication skills, both verbal and written.

  • Proficient with Microsoft Office Word and Excel.

  • Ability to work independently and prioritize duties.

  • Understanding of Electronic Data Capture (EDC).

  • Available to travel.

 

Job Type: Part-time

 

LOCATION

MILAN

 

Invia il cv con l'autorizzazione del trattamento dei dati personali in base all’art. 13 del D. Lgs. 196/2003 e all’art. 13 GDPR 679/16 ed il riferimento della posizione all'indirizzo emailuff.firenze@standler.it

L'offerta di lavoro si intende estesa a entrambi i sessi (L. 903/77). Aut. Min. Lav. prot. nr. 1417 del 22/01/2007.

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