ph3Job Summary /h3 /brpMedpace is currently seeking candidates with bPhDs and/or Post-Doctoral Research experience /b for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team.
The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities.
Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management.
/p /brpA fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and bdevelop their career in the research and development of cutting-edge therapeutics /b.
Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM).
/p /brh3Responsibilities /h3 /brul /brliCommunicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager /li /brliEnsure timely delivery of recurrent tasks consistently with a high degree of accuracy /li /brliCompile and maintain project-specific status reports within the clinical trial management system /li /brliInteract with the internal project team, Sponsor, study sites, and third-party vendors /li /brliManage and perform quality control of our internal regulatory filing system /li /brliProvide oversight and management of study supplies /li /brliCreate and maintain project timelines /li /brliCoordinate project meetings and produce quality minutes /li /br /ul /brh3Qualifications /h3 /brul /brliPhD in Life Sciences /li /brliFluency in English with solid presentation skills /li /brliAbility to work in a fast-paced dynamic industry within an international team /li /brliPrior experience within the CRO or pharmaceutical industry not required but will be advantageous /li /br /ul /brh3Medpace Overview /h3 /brpMedpace is a full-service clinical contract research organization (CRO).
We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries.
Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach.
We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective.
Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.
/p /brh3Why Medpace?
/h3 /brpPeople.
Purpose.
Passion.
Make a Difference Tomorrow.
Join Us Today.
/p /brpThe work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas.
The work we do today will improve the lives of people living with illness and disease in the future.
/p /brh3Medpace Perks /h3 /brul /brliFlexible work environment /li /brliCompetitive compensation and benefits package /li /brliCompetitive PTO packages /li /brliStructured career paths with opportunities for professional growth /li /brliCompany-sponsored employee appreciation events /li /brliEmployee health and wellness initiatives /li /br /ul /brh3Awards /h3 /brul /brliRecognized by Forbes as one of America's Most Successful Midsize Companies in ****, ****, **** and **** /li /brliContinually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility /li /br /ul /brh3What to Expect Next /h3 /brpA Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
/p /p #J-*****-Ljbffr

Associate Clinical Trial Manager (Phd) - Neuroscience / Ophthalmology

Automotive Sales Consultant - Torino

Responsabile di negozio

Ricevi nuove offerte di lavoro

Direttore Generale (M/F)

Contabile