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תוצאות חיפוש - Janssen

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משרה
ascdescחברה
ascdescמיקום
בחירה
מיקום : שפיים
בחירה
CRA

Description

CRA - Clinical Research Associate
A Site Manager serves as the primary contact point between the Sponsor and the Investigational Site.
A Site Manager is assigned to trial sites to ensure inspection readiness through compliance with the clinical trial protocol, company Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations and guidelines from study start-up through to site closure.
Responsibilities may include assisting with site selection, pre-trial assessment, subject recruitment and retention planning, site initiation, on-site and remote monitoring and close-out activities. Site Manager will partner with the Local Trial Manager (LTM), Clinical Trial Assistant (CTA) and Clinical Trial Manager (CTM) to ensure overall site management while
performing trial related activities for assigned protocols. May contribute to process improvement and training.


Principal Responsibilities

1. Acts as primary local company contact for assigned sites for specific trials.
2. May participate in site feasibility and/or pre-trial site assessment visits
3. Attends/participates in investigator meetings as needed.
4. Responsible for executing activities within site initiation and start-up, preparation and conduct of site monitoring (including remote monitoring), site management (by study specific systems and other reports/dashboards) and site/study close-out according to SOPs, Work Instructions (WIs) and policies. Responsible for the implementation of analytical risk based monitoring model at the site level and to work with site to ensure timely resolution of issues found during monitoring visits.
5. Ensures site staff are trained and the corresponding training records are complete and accurate at any time point during all trial phases. Responsible in close collaboration with LTM and central study team for the activities during site activation phase in order to speed up the process and activate the site in shortest possible timeframe.
6. Contributes to site level recruitment strategy and contingency planning and implementation in partnership with other functional areas.
7. Ensures site study supplies (such as Non-Investigational Product (IP), lab kits, etc.) are adequate for trial conduct.
8. Ensures that clinical drug supplies are appropriately used, handled and stored and returns are accurately inventoried and documented.
9. Arranges for the appropriate destruction of clinical supplies.
10. Ensures site staff complete data entry and resolve queries within expected timelines.
11. Ensures accuracy, validity and completeness of data collected at trial sites
12. Ensures that all Adverse Events (AE) /Serious Adverse Events (SAEs )/Product Quality Complaints (PQCs) are reported within the required reporting timelines and documented as appropriate. For AEs/SAEs, ensures that they are consistent with all data collected and with the information in the source documents.
13. Maintains complete, accurate and timely data and essential documents in relevant systems utilized for trial management.

14. Fully documents trial related activities, in particular monitoring. Writes visit reports and follow-up letter in accordance with the SOPs. Promptly communicates relevant status information and issues to appropriate stakeholders.
15. Reviews study files for completeness and ensures archiving retention requirements are met, including storage in a secure area at all times.
16. Collaborates with LTM for documenting and communicating site/study progress and issues to trial central team.
17. Attends regularly scheduled team meetings and trainings.
18. Complies with relevant training requirements. Act as local expert in assigned protocols. Develops therapeutic knowledge sufficient to support role and responsibilities.
19. Works closely with LTM to ensure Corrective Action Preventative Action (CAPA) is completed for Quality Assurance (QA) site audits and for quality issues identified at the site during routine monitoring and other visit types, e.g. On Site Quality Monitoring Visit (OSQMV).
20. Prepares trial sites for close out, conduct final close out visit.
21. Tracks costs at site level and ensure payments are made, if applicable.
22. Establishes and maintains good working relationships with internal and external stakeholders in particular investigators, trial coordinators and other site staff.
23. May participate in the Health Authority (HA) and IEC/IRB submission and notification processes as required/appropriate.
24. Acts as a point of contact in site management practices.
25. May contribute to process improvement and training.

Requirements

Education and Experience Requirements

A minimum of a BA or BS degree in Life Sciences, Nursing or related scientific field (or equivalent experience) is required.
A minimum of 1 year of clinical trial monitoring experience is preferred, however, other relevant experiences and skills may be considered by the hiring manager when considering the candidate’s eligibility.
Specific therapeutic area experience may be required depending on the position.
Strong working knowledge of GCP, company SOPs, local laws and regulations, assigned protocols and associated protocol specific procedures including monitoring guidelines.
Strong IT skills in appropriate software and company systems. Willingness to travel with occasional overnight stay away from home.
Proficient in speaking and writing the country language and English. Good written and oral communication.

 

 

#Gifts

Location: שפיים

Comments

Comments
Janssen is an equal opportunity employer promoting diversity and inclusion in the work place.
This position may be suitable for any person subject to their qualifications and capabilities, regardless of (inter alia) gender, origin, ethnicity, sexual orientation, and/or disability

מיקום : שפיים
בחירה
EMEA RWE Partnership Lead

Description

The EMEA Real World Evidence (RWE) team is establishing long-term partnerships with highly recognized research and data institutions across Europe. In-depth data landscape analysis and feasibility assessment is a key step when evaluating and deciding upon our continuous commitment in partnering with the data institution(s) and health system partners in scope.

In this role, you will be accountable for working collaboratively with internal and external stakeholders in linking and building data sources into a data hub, identify strategic partnerships opportunities and establish VBHC collaborations within Israel and EMEA (or even global teams as need it).
This will involve working cross-functionally to evaluating the strategic fit of and building external collaborations/partnerships that will enhance Janssen’s leadership in data access, aligned to business needs. You will collaborate with local, regional, and global RWE experts and work closely with various subject matter experts to drive internal alignment and provide recommendations to the brand teams on data opportunities and strategic alliances.

This role will be pivotal for building a regional center of excellence in setting up scientific standards for RWE research and should provide the foundation for the execution of value-based health partnerships.

Key responsibilities:

- Map and maintain landscape of current initiatives within Israel for building partnerships and create data access for Janssen EMEA.
- Continuously explore opportunities for strategic partnerships with academia, hospital networks, HMOs research institute, foster federated data networks or partner with innovative start-ups within Israel.
- Build on the current existing strategic partnership in Israel to ensuring a broader access to real world data
- Develop forward looking strategic partnerships and support mapping of RWE gaps with external RWD data sources (including supporting early portfolio gaps)
- Conduct comprehensive feasibility evaluations to provide recommendations on the value of future partnerships.
- Evaluate needs to consider the database, creating ability to answer key research questions across all therapeutic areas.
- Recommend around data sources and innovative methods questions (i.e., care pathway, disease burden, and societal impact)
- External environment and drive the debate: Build up and/or enhance a trusted collaboration with the external scientific community to facilitate a continuous communication and transfer of knowledge between the company, thought leaders and a wider group of stakeholders.
- Work closely with all internal and external stakeholders to increasing the acceptability of RWD and RWE for decision making.

Requirements

• Master’s degree and or PhD in Pharmacoepidemiology or related field (data science, epidemiology, outcomes research, public health, biostatistics)
• At least 5 years of experience in working with claims, electronic healthcare records (EHR), survey data, outcomes research, data analytics in the pharmaceutical industry or healthcare company
• Advanced knowledge and experience in conducting epidemiologic and observational research, real world research and the evaluation of health care interventions
• Comprehensive knowledge of health care system and start up/innovation ecosystem in Israel
• Extensive professional experience with RWD and VBHC partnerships and/or building data strategies at a pharmaceutical company at global, regional or operating company level
Expected behavioral traits:
• Ability to think strategically and work collaboratively with internal and external stakeholders, recognizing the potential value generated by information generated through these partnerships and the ability to communicate the value accordingly to ensure any financial and FTE commitments
• Project management capabilities. Highly collaborative as well as team player
• Excellent networking, listening, highly presentation skills, negotiation and scientific writing skills
• Open for change and flexible attitude to be able to handle a complex, multiple stakeholder environment internally as well as externally
• Seeing the big picture whilst also being very analytical and with eye for details as needed.

Location: שפיים

Comments

Janssen is an equal opportunity employer promoting diversity and inclusion in the work place.
This position may be suitable for any person subject to their qualifications and capabilities, regardless of (inter alia) gender, origin, ethnicity, sexual orientation, and/or disability
מיקום : שפיים
בחירה
Local Safety Specialist

Description

Responsible for all stages of adverse event reporting for clinical study and post-marketing drugs and products. Accountable for collecting data, investigating facts and circumstances and reporting findings to appropriate stakeholders and regulatory agencies.
Ensure the pro-active Benefit Risk Management throughout product life cycle translating global safety
data to insights and actions tailoring to local specificities and needs.
Support activities related to safety reporting requirements as required by Marketing Authorization
Holders and/or study sponsor, as applicable.

Aggregate reports
• Provide medical input and insights for aggregate reports;
• Support to ensure the submission of Periodic Safety Update Reports

PV-Safety training support
• Perform Pharmacovigilance training for Local Operating Company employees;
• Perform training for Local Operating Company employees covering (pharmacological) safety aspects of products as applicable;
• Follow up for completion of global roll out AE/PQC training in LOC.

PV contract management
• Function as IPV Lead reviewer, to have PVA implementation and oversight
• Coordinate the provision of support for third party safety agreements locally e.g. local Vendor Agreements as necessary, seek support from central functions like PV Service and Technical Contracts Group and HUB as necessary
• Provide and/ or review quarterly listings for the PSMF Annex B (vendor agreements and commercial agreements) for agreements signed by local Opco and ensure accuracy and timeliness
• Support the LSO in taking responsibility for Products of Local Opportunity (POLOs) agreements, and support the implementation of the PV agreement locally, as appropriate.

Safety regulations
• Report regulatory requirements,
• Support the review of new/revised safety regulations (for drugs and non-medicinal products in scope of responsibilities),
• Implementation of new legislations with local impact for IPV owned activities, depending on topics

Local Communications
• Work with the LSO and with Regulatory Affairs to forward any safety-related inquiry or relevant communication from the local RA to the appropriate global and regional groups (GMS Support Desk, GMS Physician, OCMS, QPPV Offices, VP PV & Medical Compliance) as appropriate. This may include local, regional and/or global expertise
• Support the Qualified Person (QP), the LSO to provide safety-related regulatory communication.

Pharmacovigilance and Vigilance Service Provision
• Collaborate with LSO to ensure that day-to-day Pharmacovigilance activities and safety activities for non-medicinal products (i.e. cosmetics, medical devices, commodities, nutritionals) are performed satisfactorily, and that full regulatory compliance is maintained at Local Operating Company level including adequate record management
• Collaborate with the local Marketing Authorization Holder (MAH) to enable fulfilment of its regulatory responsibilities (including Pharmacovigilance Agreement (PVA’s)) and meet their business objectives

Collaborate with LSO to ensure day to day safety for non-medicinal products and PV activities are performed satisfactorily including translation, follow up request.

Requirements

Certified pharmacist - B.Pharm
Clinical Safety Experience PV - Preferred
Previous experience in Pharmacovigilance and regulatory - preferred
English - very good

Temporary position with options for permanent **

Ability to work in global company with various interfaces & systems
Very good communication skills
Details oriented, ability to work with data and Excel

Location: שפיים

Comments

Janssen is an equal opportunity employer promoting diversity and inclusion in the work place.
This position may be suitable for any person subject to their qualifications and capabilities, regardless of (inter alia) gender, origin, ethnicity, sexual orientation, and/or disability
מיקום : כל הארץ
בחירה
Medical Representative

Description

Our North Area Medical Representative
will be responsible for achieving pharmaceutical product sales to new and established hospital accounts to achieve sales objectives and greater market penetration. This job is eligible for sales incentives/sales commissions.

Requirements

Relevant BA - Must
MA - Advantage
3 + experience as Medical Representative in Pharma -
Very good learning skills, can analyze clinic articles & materials
Best communication skills
English - High level
Marketing & Sales in DNA
Agility to prioritize task and lead projects
Office - PP & Excel
Valid Driving license
Location - North

Location: כל הארץ

Comments

Janssen is an equal opportunity employer promoting diversity and inclusion in the work place.
This position may be suitable for any person subject to their qualifications and capabilities, regardless of (inter alia) gender, origin, ethnicity, sexual orientation, and/or disability
מיקום : שפיים
בחירה
מנהל/ת מותג

תאור המשרה

ניהול מותג תוך הטמעת אסטרטגיות שיווק גלובליות, הוצאה לפועל של תוכניות שיווק וניהול ומעקב תוכניות הסחר של המותג על ידי המפיץ.

דרישות וכישורים

• תואר אקדמי . עדיפות למנהל עסקים/כלכלה/שיווק
• ניסיון קודם בתפקיד דומה של לפחות שנתיים (עדיפות למוצרי טואלטיקה\דנטלי\OTC).

• חשיבה אסטרטגית ויכולת הבנה עסקית של תהליכים ומטרות
• הטמעת אסטרטגיות המותג בהתאם להנחיות הגלובליות
• ניטור נתוני מכירות, נתחי שוק, מתחרים ורווחיות.
• ניהול התקשורת היומיומית עם המפיץ ומעקב עמידה ביעדים
• בניית תוכניות שיווק שנתיות והשקת מוצרים חדשים לשוק
• הוצאה לפועל של תוכניות השיווק
• בניית תוכנית מבצעים ופעילויות בנקודות המכירה בשיתוף עם המפיץ
• ניהול תקציב שיווק וסחר
• יכולת עבודה עצמאית מול ממשקים רבים במקביל ועבודה בלחץ זמן (מולטי טאסק)
• יכולת פרזנטטיבית מעולה
• אנגלית ברמה גבוהה מאוד
• יכולת אנליטית של נתונים ומגמות בשוק
• אחריות כוללת למותג ומוסר עבודה גבוה
• יכולת עבודה בצוות

מיקום: שפיים

הערות

יאנסן הוא מעסיק המקדם שוויון הזדמנויות וגיוון במקום העבודה.
משרה זו עשויה להתאים לכל אדם באשר הוא בהתאם לכישוריו ויכולותיו, בין היתר, ללא קשר למגדר, מוצא, שיוך אתני, נטיה מינית ו/או מוגבלות.

מיקום : שפיים
בחירה
LTM - Local Trial Manager

Description

Global Clinical Operations (GCO)
Position Title*: Local Trial Manager II
Position Summary:

The Local Trial Manager II (LTM II) is responsible for local management of a clinical trial (or Medical Affairs data generation activity) in a country or countries. The LTM II is the primary point of contact at a country level for assigned studies and has operational oversight of assigned protocol(s) from start-up through to database lock and closeout activities as described in GCO procedural documents. The LTM II is responsible for coordinating and leading the local trial team to deliver quality data and trial documents/records that are compliant with the assigned clinical trial protocol, company Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and regulatory requirements.
The LTM II actively contributes to process improvement; training and mentoring of Clinical Trial Assistants (CTA), Site Managers (SM) and LTM I roles. The LTM II may have some site management responsibilities.
The LTM II may also perform the role of Clinical Trial Manager (CTM)/Global Trial Lead (GTL) for single country as described in GCO procedural documents.

Requirements

Principal Responsibilities:

1. Collaborate with Functional Manager (FM)/Clinical Research Manager (CRM) for country protocol feasibility (if applicable) and site feasibility assessment in conjunction with CTA (if applicable), SM and CTM/GTL. Implements any local criteria for site selection. Ensure consistent conduct of pre-trial assessment visits and instruct teams on appropriate follow-up of pre-trial visit report and country feasibility report. Recommends suitable sites for selection to participate in trial.
2. Collaborates with the Global Product Lead (GPL), CTM/GTL, local management/Country Head and other study team member to select final site list.
3. Contributes input to the study management documents at a country level or initiates development of these documents for a single country trial, as per SOPs
4. Leads and coordinates local trial team activities in compliance with SOPs, other procedural documents and applicable regulations. Leads local project planning activities to meet recruitment targets and to deliver high quality data on time and within study budget. Including but not limited to: development of local trial specific procedures and tools, recruitment planning, contingency and risk management, and budget forecasting.
5. Ensures that all Adverse Events (AE) /Serious Adverse Events (SAEs)/Product Quality Complaints (PQCs) are reported within the required reporting timelines and documented as appropriate.
6. Maintains and updates trial management systems. Uses study tools and management reports available to analyse trial progress
7. Monitors country progress and initiates corrective and preventive actions (CAPA) when the trial deviates from plans and communicates study progress and issues to study management teams.
8. May submit requests for vendor services and may support vendor selection.
9. In certain situations, may assist in negotiation of trial site contracts and budgets. Forecasts and manages country/local trial budget to ensure accurate finance reporting and trial delivered –within budget. Adheres to finance reporting deliverables and timelines.
10. Attends/participates in Investigator Meetings as needed. May schedule and conduct a local/country investigator meeting
11. Conducts local trial team meetings and provides or facilitates SM training when needed (i.e. implementation of study amendment-and changes in study related processes).
12. Reviews and approves Monitoring Visit Reports submitted by SM; identifies issues and/or trends across a trial project and escalates deviation issues to the CTM/GTL and FM as needed
13. Reviews and approves site and local vendor invoices as required. Manages local study supply, as required.
14. Prepares country specific informed consent in accordance with procedural document/templates.
Reviews and manages site specific informed consent forms in accordance with SOPs, other procedural documents and applicable regulations.
15. Organizes and ensures IEC/HA approvals, if applicable, and ensure that the trial is in compliance with local regulatory requirements
16. Works with SM to ensure CAPA is implemented for audits and inspection or any quality related visits
17. Complies with relevant training requirements.
18. Acts as subject matter expert for assigned protocols. Develops strong therapeutic knowledge to support roles and responsibilities. May represent GCO on cross functional teams.
19. Acts as primary local/country contact for a trial. Establishes and maintains excellent working relationships with external stakeholders, in particular investigators, study trial coordinators and other site staff; and internal stakeholders, including Medical Affairs and Marketing for Medical Affairs trials.
20. Actively contributes to process improvement, training and mentoring of CTAs, SM and other LTMs.
21. Conducts accompanied site visits with SM as delegated by FM.
22. May assumes additional responsibilities or special initiatives such as “Champion” or “Subject Matter Expert”.
23. May represents functional area in process initiatives as required

Education and Experience Requirements:

A minimum of a BA or BS degree in Life Sciences, Nursing or related scientific field (or equivalent experience) is required.
Minimum two to four years of pharmaceutical and/or clinical trial experience is preferred (including site monitoring experience), however other relevant experiences and skills may be considered by the hiring manager when considering the candidate’s eligibility.
Specific therapeutic area experience may be required depending on the position. Should have solid understanding of the drug development process including GCP and local regulatory requirements.
Willingness to travel with occasional overnight stay away from home.
Solid leadership skills. Solid communication and computer skills required. Proficient in speaking and writing
the country language and English language. Excellent written and oral communication skills
Experience in mentoring/coaching and providing training to other LTMs, SMs and CTAs preferred. The ability to lead initiative/small teams.
Flexible mindset and ability to work in a fast-changing environment. Ability to work on multiple trials in parallel.

Location: שפיים

Comments

Janssen is an equal opportunity employer promoting diversity and inclusion in the work place.
This position may be suitable for any person subject to their qualifications and capabilities, regardless of (inter alia) gender, origin, ethnicity, sexual orientation, and/or disability

אדמיניסטרטור/ית - חטיבת מוצרי הצריכה

תאור המשרה

לחטיבת שיוווק מוצרי הצריכה Consumer
דרוש/ה עוז/רת אדמיניסטרציה ושיווק
• מתן שירות שוטף לצוות השיווק מנהליו וממשקי היחידה.
• ארגון פגישות וישיבות מרובות משתתפים, תכתובות מול חו"ל.
• עבודה מול ספקים, חשבוניות ומעקבים שוטפים.
• קשר עם מפיצים בהיבטי אדמין.
• טיפול בתוויות מוצרי החברה, רגולציה, חברות דפוס ועוד.
• תמיכה תפעולית של אתר החברה ודיגיטל.

דרישות וכישורים

• תואר ראשון - חובה
• עברית שפת אם אנגלית גבוהה, כולל יכולת התנסחות גבוהה.
• ניסיון אדמיניסטרטיבי מחברה גלובאלית - יתרון מובהק.
• זיקה / ניסיון קודם בתחום השיווק.
• יישומי מחשב ברמה גבוהה לרבות ניהול יומנים ורשתות חברתיות.
• ניסיון בעבודה עם ספקים / מפיצים, חשבוניות - יתרון.
• יחסי אנוש גבוהים, שירותיות גבוהה, אמינות ואחריות אישית.
• יכולת עבודה בריבוי משימות, יכולת עבודה עצמאית ובשיתוף.

מיקום: שפיים

הערות

*המשרה בהעסקה חיצונית, משרה קבועה במשרדי יאנסן, שפיים.

*ג'ונסון & ג'ונסון הינה מעסיק המקדם שוויון הזדמנויות וגיוון במקום העבודה.
משרה זו עשויה להתאים לכל אדם באשר הוא בהתאם לכישוריו ויכולותיו, בין היתר, ללא קשר למגדר, מוצא, שיוך אתני, נטיה מינית ו/או מוגבלות.
מיקום : שפיים
בחירה
Medical Advisor- Hemato-oncology

Description

Master and Lead the scientific communication - Lead the medical and scientific knowledge of the drug and its indications: Knowledge of all relevant publications (TA, product and competitors) and on-going studies of the company’s products and competitors in selected therapeutic areas.
Support medical and scientific initiatives associated with the company's products, new indications and late stage clinical development candidates
Lead and conduct Scientific educational presentations to healthcare providers (physicians, nurses, pharmacists) in ward / staff / journal club meetings.
Initiate and facilitate medical education activities - Developing educational contents, Planning and organization of educational workshops, seminars, programs and advisory boards (clinical discussion & debating forums) for physicians, pharmacists and scientists.
Attending assigned medical and scientific local and international meetings to respond to inquiries from the medical community, addressing current scientific issues and new data pertaining to the company’s products.
Conducting sophisticated, appropriate scientific interchange with Key Opinion Leaders (KOL’s).
Involved in strategy planning and activities related to products submitted for reimbursement (Health Basket).
Developing on-going professional relationships with national healthcare practitioners to provide medical and scientific support for the company’s initiatives in selected therapeutic areas.
Providing training / scientific coaching to the business units.
Being Medical and scientific resource for health care providers based on sales force feedback and customer requests.

Requirements

MD, PhD (life Science), DVM, DMD (Israeli license) - Must
Strength in research and Interpretation of medical data.
Deep knowledge of the therapeutic area – an advantage.
Previous role as a Medical Advisor- an advantage.
Excellent people skills.
Excellent service orientation.
Ability to multi-tasking.
Team Player.
Ability to learn new processes and applications “on-the-fly”.
Good organizational and project planning skills.
Excellent presentation skills.
An active vibrant and agile team player of the functional brand team.

Location: שפיים

Comments

Janssen is an equal opportunity employer promoting diversity and inclusion in the work place.
This position may be suitable for any person subject to their qualifications and capabilities, regardless of (inter alia) gender, origin, ethnicity, sexual orientation, and/or
מיקום : שפיים
בחירה
RA Specialist

Description

Position Summary

The responsibility of the ERMC RA Lifecycle Management (LCM) is to coordinate a broad range of product lifecycle changes for multiple countries in the EMEA region, from planning of the submission up to implementation of the change in the applicable databases and artworks.
The current job opening is for a LCM RA Professional for the Non-EEA region for Israel submissions.

Job description

Janssen is looking for a talented, experienced regulatory affairs professional to join the EMEA RMC (ERMC) team. The role is to focus primarily on the coordination of procedures within the ERMC team; ensuring compliant, high quality and timely submissions to the Health Authorities for lifecycle management activities for Janssen products. The successful candidate will be dedicated to a cluster of countries and will work closely together with local and regional project teams.

The ideal candidate will bring in this role a high level of awareness of the applicable regulatory environment. The candidate will further require a pro-active attitude, problem-solving capabilities and excellent communication skills.

Requirements

Relevant BA - Must
RA Experience - at least 3 years - Pharma

Ability to work in English - Additional Languages - advantage
Good communication and organizational skills, team player

**Temporary Position

Location: שפיים

Comments

Janssen is an equal opportunity employer promoting diversity and inclusion in the work place.
This position may be suitable for any person subject to their qualifications and capabilities, regardless of (inter alia) gender, origin, ethnicity, sexual orientation, and/or disability


מיקום : שפיים
בחירה
Product Manager- IMBRUVICA

תאור המשרה

Product Manager- IMBRUVICA

יחידה עסקית: המטו-אונקולוגיה

תיאור המשרה:
מנהל/ת מוצר- אימברוביקה

אימברוביקה היא טיפול פורץ דרך אשר מוכיח את יעילותו במספר רב של סרטני דם. הטיפול זמין בישראל עבור חולים המטו-אונקולוגיים בחמש מחלות שונות, ולצד זה נמצא במחקר לשימושים שונים שעדיין לא הגיעו אל השוק.

תפקיד מנהל/ת המוצר כולל:
• קידום הטיפול בכל ההתוויות הזמינות בישראל,
• עבודה אינטנסיבית בממשקים מגוונים עם שותפים בתוך צוות אימברוביקה, ביחידה ההמטו-אונקולוגית ובחברה בכלל.
• חשיבה אסטרטגית ובניית אסטרטגיה תחרותית המותאמת לשוק דינמי ומתפתח.
• בנייה והוצאה לפועל של תכנית טקטית למינוף ההזדמנויות והתמודדות עם האתגרים בשוק, כולל תכנית תקשורת רב-ערוצית עם לקוחות.
• ניהול נפח פעילות רחב של עשיה בתחום ההמטולוגיה - יכולת הנעת פרויקטים, חשיבה יצירתית, מתן מענה ללקוחות במגוון תחומים ויוזמה מתמדת.
• השקה של התוויות עתידיות ומיצובן לצד הקיים.


דרישות וכישורים

השכלה:
• תואר ראשון במדעי החיים או במקצוע פרה רפואי אחר – הכרחי
דרישות:
• ניסיון בניהול מוצר בתחום הפארמה בחברה בינ"ל- חובה!
• יתרון משמעותי לניסיון בתחום ההמטולוגיה/אונקולוגיה
• שליטה בשפה האנגלית
• רישיון נהיגה בתוקף
דרישות נוספות:
• יכולת ניהול והובלה
• יכולת עבודה בממשקים רבים
• יכולת ניהול של מגוון משימות בו זמנית
• ניסיון בחשיבה אסטרטגית, בבניית תכנית אסטרטגית לטווח ארוך
• יכולת הבנה וניתוח מאמרים מדעיים מקצועיים

מיקום: שפיים

הערות

יאנסן הוא מעסיק המקדם שוויון הזדמנויות וגיוון במקום העבודה.
משרה זו עשויה להתאים לכל אדם באשר הוא בהתאם לכישוריו ויכולותיו, בין היתר, ללא קשר למגדר, מוצא, שיוך אתני, נטיה מינית ו/או מוגבלות.