Covance Start-up Specialist II in Rome, Italy
Get ready to redefine what’s possible and discover your extraordinarypotential at Covance. Here, you’ll have the opportunity to personally advance healthcare and make a difference in peoples’ lives with your bold ideas and unique point of view. With the support of exceptional people from across the globe and an energized purpose , you’ll be empowered to own your career journey with mentoring, training and personalized development planning.
Join us as we speed the delivery of groundbreaking therapies and anticipate tomorrow’s drug development challenges, creating new possibilities for our clients—and your career.
We are currently seeking a proactive, driven Start-up Specialist II to join our expanding team in Rome, Italy .
You will have a great opportunity to develop yourself and also to learn from the best.
Act as the lead contact with investigative sites during assigned site start-up activities
Oversee timely collection of the required investigator and regulatory documents for a study as specified by regulatory authorities and sponsor
Ensure the ongoing accuracy and quality of site/study documents.
Ensure high quality documents are filed in (e)TMF and systems are updated on an ongoing basis ensuring Covance is audit ready at any time.
When applicable, work with staff in Business Development and Operations, to provide relevant input critical to successful trial execution
Provide accurate projections and timelines to study teams based upon country’s historical performance and agreed with Sponsor
Ensure project plans are followed for the Site Activation component of assigned studies, proactively engaging with key stakeholders to assure milestones are adequately represented and are being achieved and driving for solutions.
Participate in team meetings to report progress and challenges in trials. Identify potential risks to timelines and results and manage issues independently.
Review and customize country and site specific patient informed consents for compliance with local requirements and protocol
Proactively resolve informed consent issues and other potential difficulties with study sites.
Monitor start up activities to ensure issues are identified, managed and, if necessary, escalated to the appropriate individual.
May negotiate contracts and budgets with investigative sites within parameters provided by SU PM and Sponsor.
Liaise with Covance Regulatory department regarding document submission requirements, if applicable
When needed review data for feasibility assessments at a country level.
Coach less experienced study team members as appropriate.
May be asked to negotiate timelines or delivery of project plan with SUPM’s under direction of senior specialist/SUCM
Perform other duties as assigned by management
Education / Qualifications
University/College degree (life science preferred), or certification in a related allied health
profession from an appropriate accredited institution (e.g., nursing certification, medical or
laboratory technology) AND 2 years work experience in clinical research, including a strong
working knowledge of the ICH guidelines and FDA, IRB/IEC regulations.
In lieu of the above requirement, candidates with a High School Diploma or equivalent AND a
minimum of 4 years work experience in clinical research, including a strong working knowledge of the ICH guidelines and FDA, IRB/IEC regulations will be considered.
Minimum of 4 years of experience in clinical development or regulatory process.
Significant experience of applying strong knowledge of ICH, FDA, IRB/IEC and other applicable
regulations/guidelines; familiarity with investigator start-up documents and contract/budgets
negotiation process; previous interaction with operational project teams and investigative sites
Significant experience of issue escalation and resolution.
Proven track record of effective communication and problem solving.
Experienced in creating and maintaining good business relationships
Proven ability to work under pressure with multiple internal clients with competing goals
THERE IS NO BETTER TIME TO JOIN US!
Job Number 2018-18993
Job Category Clinical Operations
Position Type Full-Time
Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran/Sexual Orientation/Gender Identity). Your confidentiality and privacy are important to us.