Clinical Research Associate

2 settimane fa


Roma, Italia Optimapharm A tempo pieno

Location: home-based Who are we? Optimapharm is a leading, mid-sized, full-service CRO working across Europe and North America to deliver new therapies to improve and save patients’ lives. Optimapharm’s key priorities are our people and consistently exceeding our client’s expectations. With 27 strategically located offices , Optimapharm operates in 40+ countries, giving unrivaled access to Patients and Investigators in all countries in Europe and North America. In-depth expertise and long-standing experience, combined with a flexible and collaborative approach, allow optimization of design and planning; through its strong track record of delivery excellence and committed and stable project teams, Optimapharm has secured a high level of repeat business over the years. We are looking for a Senior CRA/CRA III to join our Clinical Operations team in Italy and support us in making a tangible difference to project sponsors and benefiting patients and their families all around the world. What do we offer? Working in a successful company that’s growing and changing every day Working with a highly experienced team of clinical research professionals International projects and professional growth Performance bonus Referral bonus Training opportunities Flexible work hours Home-based position Summer work schedule Working from home allowance Meal vouchers Shopping discounts Who are we looking for? Qualifications and Experience Master's degree (5-year program), preferably in medical or life sciences . Individuals with a university degree in biotechnical, technical, bio-medicinal, social, or humanistic sciences must have a nursing education or other relevant healthcare college degree. At least 3 years of independent clinical trial monitoring experience Experience in oncology and start-up activities is an advantage High level of knowledge of ICH GCP Guidelines, knowledge of regulatory requirements, and a strong interest in clinical research Fluent in local language and English ; both, written and verbal Computer proficiency is mandatory Ability to read, analyze, and interpret common scientific and technical journals Excellent verbal and written communication skills Very good interpersonal and negotiation skills Ability to work with minimal supervision, proactive Affinity to work effectively and efficiently in a matrix environment Excellent numerical skills and reasoning ability A current, valid driver’s license would be advantageous Your responsibilities Perform routine site visits with minimal guidance, including pre-study, initiation, interim monitoring, and closeout visits Manage assigned sites by regular contact with site personnel to ensure site compliance, adequate enrolment, and understanding of study requirements Independently perform CRF review; query generation and resolution against established data review guidelines or data management systems as applicable Identify and escalate potential risks and identify retraining opportunities for site personnel Preparation of corrective and preventive (CAPA) plans for issues identified during monitoring activities and pro-active follow-up of each individual CAPA until timely resolution Preparation of documents required for EC submissions and notifications, translation of study-related documents (where applicable), and other tasks as instructed by the supervisor With minimal supervision, negotiate study budgets with potential investigators/institutions and assist with the execution of site contracts as applicable Administration of site payments in accordance with relevant project instructions By joining our fast-growing and prosperous team, you will have an excellent opportunity for further personal growth and career development. If you would be interested in joining the Optimapharm team, please send your CV in English and note that only shortlisted candidates who meet the requirements will be contacted for the further selection process. #J-18808-Ljbffr



  • Roma, Italia EastHORN Clinical Services A tempo pieno

    **Job summary**: As a **Clinical Research Associate **you will be expected to actively participate in and manage the recruitment of potential investigators and perform CA and EC submissions. You will be responsible for monitoring of clinical sites, maintenance of study files, conduct of pre-study and initiation visits, liaison with vendors and other duties....


  • Roma, Italia IQVIA LLC A tempo pieno

    Clinical Research Associate, Site Management - Italy page is loaded Clinical Research Associate, Site Management - Italy Apply locations Milan, Italy time type Full time posted on Posted Yesterday job requisition id R1415148 Job Overview Engage in structured training program to gain knowledge and skills required to independently conduct clinical monitoring...


  • Roma, Italia Barrington James A tempo pieno

    Clinical Research Associate III - Ophthamology - Italy Job Overview: As a Senior CRA specializing in ophthalmology, you will play a crucial role in the planning, implementation, monitoring, and management of clinical trials related to ophthalmic drugs, devices, or therapies. You will ensure that clinical trials are conducted in accordance with applicable...


  • Roma, Italia Barrington James A tempo pieno

    Clinical Research Associate II - Ophthamology - Italy Job Overview: As a Senior CRA specializing in ophthalmology, you will play a crucial role in the planning, implementation, monitoring, and management of clinical trials related to ophthalmic drugs, devices, or therapies. You will ensure that clinical trials are conducted in accordance with applicable...


  • Roma, Italia ABBVIE A tempo pieno

    **Key responsibilities**: - Monitors activities conducted by clinical investigative sites as they relate to AbbVie clinical studies to ensure successful execution of the protocol. Ensures adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), Monitoring...


  • Roma, Italia Novo Nordisk A tempo pieno

    The Italian affiliate of Novo Nordisk, based in Rome, is hiring a Clinical Research Manager (CRA Team Manager). Do you want to join one of the leading companies of the pharma sector? Do you want to build your career and contribute to the growth and development of the company? We're on the lookout for a knowledgeable, proactive, dedicated people manager to...


  • Roma, Lazio, Italia University of Liverpool A tempo pieno

    Following a successful grant application to the UK Arts and Humanities Research Council we are seeking to recruit one 60% FTE (i.e. 3 days per week) Postdoctoral Research Associate, for a 9-month fixed period, based in Rome, Italy.The Project entitled The Other Rome: Centring People and Spaces of Maintenance is a collaboration between the Liverpool School of...


  • Roma, Italia Fortrea A tempo pieno

    Clinical Research Manager - Home Based Italy As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20...


  • Roma, Italia United States Institute for Theatre Technology A tempo pieno

    Clinical Associate Professor (Scenery/Props) Sands College of Performing Arts at Pace University is seeking a full-time Associate Clinical Professor to teach design and stagecraft courses (independently or collaboratively) and maintain a high level of support for the artistic production and academic goals of students and the University, including mentoring...


  • Roma, Italia GSK A tempo pieno

    **Site Name**: USA - Maryland - Rockville, Belgium, Italy **Posted Date**: May 11 2023 Are you energized by an opportunity to accelerate and deliver a Clinical Sciences Strategy that drives compliance and efficiency? If so, this Associate Director, Clinical Sciences Lead (CSL) role could be an exciting opportunity to explore. Innovation is the beating...

  • Clinical Specialist

    1 settimana fa


    Roma, Italia Masimo A tempo pieno

    Central Italy**Job Summary**: The Clinical Specialist is an entry level role responsible for supporting Masimo Products and maintaining customer relationships with a variety of clinicians and other key stakeholders. **Duties & Responsibilities**: - You will be seen as an expert in pulse oximetry and pulse CO-Oximetry as well as an authority on the clinical...

  • Clinical Specialist

    2 settimane fa


    Roma, Italia Masimo Corporation A tempo pieno

    Central Italy Job Summary: The Clinical Specialist is an entry level role responsible for supporting Masimo Products and maintaining customer relationships with a variety of clinicians and other key stakeholders. Duties & Responsibilities: You will be seen as an expert in pulse oximetry and pulse CO-Oximetry as well as an authority on the clinical impact...


  • Roma, Italia Parexel International A tempo pieno

    At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that...


  • Roma, Italia Novo Nordisk A tempo pieno

    Clinical Innovation & Implementation Manager **Category**:Clinical Development**Location**:Roma, Lazio, IT- **The Position** - As our Innovation and Implementation Manager, you will be responsible for leading and implementing innovative clinical projects, as well as tracking and analysing clinical activities throughout CDC Italy, with the aim of maximizing...

  • Associate Professor

    4 settimane fa


    Roma, Italia Ningbo University A tempo pieno

    All successful applicants can expect: - a one-off funding of 1 million RMB (~140K USD) for full time/ 0.5 million RMB (~70K USD) for part time for individual - weekly salaries starting from 15K RMB ~ 50K RMB (~2.5K to 7K USD) for individual * * Position: Positions are open at five distinct ranks: Postdoctoral Fellow,Assistant Professor, Associate...


  • Roma, Italia Randstad Italia Spa A tempo pieno

    Mansione Hai esperienza in ambito di processi di sintesi organica? Appartieni alle categorie protette secondo articolo 1 della legge 68/99? Randstad Talent Selection Hopportunities è la divisione specializzata nella Ricerca &, Selezione di professionisti qualificati appartenenti alle categorie protette. Ricerchiamo Research Associate per primaria realt...

  • Senior CRA

    2 settimane fa


    Roma, Italia Barrington James Limited A tempo pieno

    Barrington James is actively recruiting for a challenging role as a Clinical Research Associate (CRA II). As part of our clients in-house team, you will be responsible for site management, encompassing start-up activities both on-site and remotely across Italy. This role involves working on diverse projects from our client base, which includes small to...


  • Roma, Italia ICON A tempo pieno

    ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development...


  • Roma, Italia IRBM S.p.A. A tempo pieno

    IRBM is a drug discovery and development company with a track record of success in accelerating and executing the translation of novel discoveries into clinically relevant therapeutic entities, including small molecules, peptides and monoclonal antibodies. IRBM is headquartered in Pomezia (Rome), Italy and provides several integrated pre-clinical laboratory...


  • Roma, Italia Air Force Research Laboratory A tempo pieno

    Assists in the design, integration, and documentation of software interfaces, APIs, and libraries to address the complexities of modern military decision making. Assists in performing professional computer science work of limited scope and complexity in support of research or projects. Applies a number of computer science practices, techniques, and...