Descripción del trabajoDo you get energy from coordinating dynamic clinical trials with a quality-driven and pragmatic approach? Do you like to partner with many stakeholders? Do GCP ICH E6 R3 and ISO 14155 have no secrets anymore for you? You might be the
Sea uno de los primeros solicitantes, lea la descripción completa del puesto a continuación y luego envíe su candidatura para que sea considerada.
Clinical Project Manager
we are looking for at QbD Clinical!
What you’ll be doing
Strategizes, oversees and coordinates successful execution
clinical studies .
Ensures that the rights and well-being of subjects are protected, that the reported study data are accurate, complete, and verifiable from source documents, and that the study is conducted in accordance with protocol, standard operating procedures, ISO/GCP and other applicable
regulatory requirements.
Is responsible for the overall documentation and adequacy of conduct, data quality, compliance and adherence to timelines for their assigned trial(s).
Oversees
quality of data collection , management of study supplies and resources in adherence with the project timelines, budget and quality standards
Oversees start-up, enrollment, follow up and closure of clinical trial activities
Develops clinical study protocols
and reviews/approves supporting documentation (such as monitoring plan, study plan, data management plan etc.)
Develops patient recruitment and
retention plans
Develops solutions to a variety of complex problems of diverse scope and complexity where analysis of data requires evaluation of identifiable factors.
Establishes and cultivates a wide range of
business relationships
to facilitate completion of assignments
Interacts with and manages vendors and stakeholders, as required
Determines
goals and objectives
for projects
Leads projects within the function or department and/or represents a specialized field in larger project teams. Influences middle management on business solutions.
Represents the organization as a prime contact on contracts or projects. Develops and manages the
study budget . Overall responsibility for negotiation of financial aspects of clinical studies / program.
Uses discretion, diplomacy and tact to
resolve difficult situations . Escalates serious issues to management.
What you bring
Master degree in
biological or (para-) medical sciences
or equivalent by experience
Minimum of 7 years’
experience in clinical research
or relevant experience
Minimum of 3 years’
experience as Clinical Project Leader
and previous experience as a CRA is a plus
Excellent oral and written communications skills
Excellent interpersonal skills, inspirational and motivational skills
Demonstrates
ability to manage and oversee projects
and related team activities
Demonstrates ability to make timely and well-reasoned decisions
Demonstrates ability to identify and
adapt to shifting priorities
and competing demands
Ability to maintain composure in difficult circumstances and sensitive to cultural differences
Fluent in
English . Other languages are a plus
What’s in it for you?
QbD Group offers you an
attractive and competitive salary package , that will be tailored to individual needs, considering legal requirements and local laws and regulations.
Join us to build a
sustainable career , where job security is ensured, and lasting, meaningful connections are formed.
As we’re a
knowledge-based company , you’re guaranteed to embark on a continuous journey of learning and development. xcskxlj
Be part of our global success story. As an
award-winning company
we value everyone’s contribution and celebrate achievements together
Who you are
You’re
resilient
and tackle challenges with a positive mindset
You’re
curious
and always up for learning something new
You have a
no-nonsense approach
honest, clear, respectful
You’re
innovative
and bring ideas, not just opinions
And above all, you’re
serious about your work, but not too serious about yourself
#J-18808-Ljbffr