Experienced Clinical Project Manager
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Job Location:
Monthly Salary:
Posted on:
5 hours ago
Vacancies:
1 Vacancy
Job Summary
Location: Hybrid
Type: Full-time
Do 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 Clinical Project Manager we are looking for at QbD Clinical!
What youll 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
Whats 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 were a knowledge-based company youre guaranteed to embark on a continuous journey of learning and development.
Be part of our global success story. As an award-winning company we value everyones contribution and celebrate achievements together
Who you are
Our culture is driven by values If this sounds like you youll fit right in:
Youre resilient and tackle challenges with a positive mindset
Youre curious and always up for learning something new
You have a no-nonsense approach honest clear respectful
Youre innovative and bring ideas not just opinions
And above all youre serious about your work but not too serious about yourself
About us
We support life sciences companies from idea to patient offering tailored solutions in development clinical regulatory compliance production and distribution. With 500 experts across 8 countries we help drive innovation in ATMP biotech medical devices diagnostics digital health and pharma.
We believe in JPEG:
Joy. Partnership. Going the Extra Mile. Getting Things Done.
You wont just be taking a job youll be joining a community where people grow laugh build and contribute to something bigger.
Interested Lets talk.
Send us your CV and motivation letter. You could be the next one to join the QbD family.
