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Emploi: patient access program and supply lead:Randstad.ch

Job description:


job details


publié
   . 27. octobre 2021
lieu
   . basel, bâle-ville
secteur
   . life sciences
type d'emploi
   . contract
référence
   . 16674
contact
   . audrey bisch, bâle professionals health care & life sciences
téléphone
   . 058 201 55 50
appliquer >
email

description du poste


Do you want to work in a big pharmaceutical company? Do you have at least 5 years experience in Clinical Trial Settings? You should then read the following lines! 
Our client, based in Basel, is looking for a Patient Access Program and Supply Lead for a 1 year contract.
General Information:
?       Start date: ASAP
?       Latest possible start date: 1 month notice period
?       End date: 1 year duration
?       Extension: possible
?       Workplace: Basel
?       Workload: 100%
?       Remote/Home Office: Flexible between onsite and home office.
Tasks & Responsibilities 
?       Takes the lead in projects and programs: manages project and budget management activities (develops work plans, coordinates project on day-to-day basis, tracks deliverables / milestones, facilitates clear communication between all team members and stakeholders, provides status updates, ensures adherence to high quality of deliverables)
?       Jointly develops working practices and processes related to PAPs, and maintains them up-to date, identifying and aligning strategic and operational aspects (e.g. decision-making, systems, roles & responsibilities)
?       Proactively incorporates learnings and recommendations from other programs; identifies needs for process standardization, regulatory compliance direction and areas for improvement
?       Continuously updates key process documents, incl. SOPs, supporting documents for the development of PAP procedures.
?       Establishes, maintains and fosters strong effective relationships with key stakeholders such medical colleagues in PD(MA), CoP members in MAO, GPS, Technical/Clinical Drug Supply colleagues, Quality, PV, Finance and affiliate team and vendors.
?       Ensures an efficient, effective and compliant PAP and Drug Supply management with documentation and reporting/metrics in PAIRS and other databases as required:
?       Ensures receipt, filing and tracking of PAP records (SDEAs, Physician?s Agreement, Regulatory Forms, other country specific documents) in the required quality in PAIRS.
?       Identifies and adapts PAIRS system to the needs of the various customer groups and ensuring compliance. Manages Affiliate sharepoints (filing area, affiliate area) and RecPoint (records) program area according to global standards, including set up, access rights and maintenance of program related documents;
?       Manages timely interaction between clinical program and the Clinical Demand and Supply Leads in Pharma Technical in order to ensure proper preparation and delivery of the drug supply.
?       Consolidates and monitors clinical drug supply planning for managed global and local clinical trials & programs
?       Ensures clinical drug supply budget forecasting and tracking for assigned Therapeutic Areas.
?       Acts as IXRS implementation coordinator.
?       Identifies proactively potential delivery issues and risks and ensures corrective and preventive actions (CAPAs) in case of deviation, communicates to stakeholders.
?       Supports the CoPLs in PDMA MAO to ensure PDMA representation in cross-functional / departmental initiatives related to patient access to drug. 
Must Haves:
?       Min 5 years? experience in pharma / clinical research (preferably in clinical trials) 
?       Previous project / program management experience in pharma in international clinical trials setting 
?       Experience and understanding of global expectations of Health Authorities and overall healthcare environment (ICH/GCP) 
?       Experience in multicultural & cross functional environment 
?     Soft skills are highly important here and will be evaluated during the interview stage: excellent communication skills, collaborative, pro-active and flexible mindset. 
Do not waste any minutes, apply now!  We are looking forward to receiving your application. 
Please note that only candidates with a valid work permit or who are EU/EFTA citizens will be considered.

Skills:

Job Category: Legal [ View All Legal Jobs ]
Language requirements:
Employment type:
Salary: Unspecified
Degree: Unspecified
Experience (year): Unspecified
Job Location: autre
Company Type Employer
Post Date: 03/12/2024 / Viewed 6 times
Contact Information
Company: Randstad.ch


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