Clinical Project Manager (Hybrid)
at CellCarta
2610 Wilrijk, Antwerpen, Belgium -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 04 Sep, 2024 | Not Specified | 06 Jun, 2024 | N/A | Excel,Microsoft Office,Medicine,Biomedical Sciences,Pharmaceutical Sciences,It,Critical Thinking,Powerpoint,Writing,Communication Skills | No | No |
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Description:
CLINICAL PROJECT MANAGER
Are you looking for an exciting new career opportunity? CellCarta, a renowned Contract Research Organization, is actively seeking a highly skilled and motivated Clinical Project Manager to join our dynamic team. As a Project Manager, you will have the opportunity to use your expertise and skills to ensure that our services meet the highest industry standards. Come work with a team of talented individuals who are committed to making a positive impact on human health and well-being. Apply today!
SUMMARY
As a Project manager, you will drive and manage projects with internal stakeholders and external customers (pharma and biotech partners in oncology) in order to deliver results on time in full and in agreement with the CellCarta Quality System.
As a CellCarta Clinical Project Manager (CPM), you will learn the entire business model and you will usually be the first to discover what our customers need. As a CellCarta CPM, you’re ultimately responsible for embodying 3T’s. Always keep the project on Task, on Track and on Time.
You will need to be comfortable doing the following:
- Listen well to the customer and build relationships to establish client satisfaction
- Manage yourself well under pressure
- Prioritize being effective over being right
- Be willing to transform yourself
- If you are organized, analytically minded, possess a solid technical background and will thrive in our dynamic, high complexity environment, this might just be the role you are looking for.
REQUIRED EDUCATION
- A Master degree in Sciences, Biomedical Sciences, Pharmaceutical Sciences, Medical Biology, Medicine or similar expertise through experience.
QUALIFICATION AND SKILLS
- 2+ years of project management, and/or CRA (clinical research associate) experience, or a history of working with histo-technology laboratories
- A great curiosity and a learning appetite that is layered on top of a humble and teachable spirit
- Prior success managing (complex) projects to completion with rave reviews and can pull off that delicate balancing act of prioritizing multiple opportunities
- Pro-level communication skills, proficient in English language, including writing and articulating your case
- Proficient in Microsoft Office (Word, Excel, PowerPoint, PowerBI)
- Excellent organizational skills and able to multi-task
- Positive and energetic attitude
- Able to take initiative, be adaptable, and strive in a dynamic environment
- Diligence and strong attention to detail
- Ability to work independently and as a team member
- Possesses critical thinking and problem solving skills
- Customer and Project Manager service oriented
- A solution mindset and an unrelenting stick-with-it outlook
Responsibilities:
RESPONSIBILITIES
The CPM is responsible for the delivery of clinical projects within the agreed scope, time and budget, primarily by coordinating a multitude of tasks performed by internal and external partners. The CPM ensures that the project is accomplished within the quality system of CellCarta. His/Her responsibility starts when a clinical project is granted to CellCarta and finishes when the project is delivered to the sponsor, study properly archived and final invoicing prepared.
ADDITIONAL RESPONSIBILITIES ARE:
- Manage clinical studies from initiation, all the way through close-out and archiving, including reporting, in compliance with GCP guidelines and regulations.
- Review of all required essential documents necessary for study initiation and ensure audit ready study files throughout the duration of the study
- Prepare and/or approve design sample flows; study trackers; Bio-Analytical Report; and other required documents for clinical studies
- Study budget control
- Maintain and document professional communication with the sponsor; cross functional project team and management throughout the duration of the study
- Chairing sponsor calls
You will need to be comfortable doing the following:
- Listen well to the customer and build relationships to establish client satisfaction
- Manage yourself well under pressure
- Prioritize being effective over being right
- Be willing to transform yourself
- If you are organized, analytically minded, possess a solid technical background and will thrive in our dynamic, high complexity environment, this might just be the role you are looking for
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Biology
Proficient
1
2610 Wilrijk, Belgium