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Medical Advice and Communications Specialist - Pharmaceuticals

Eingestellt von Elevate Direct

Gesuchte Skills: Support, Network

Projektbeschreibung

MEDICAL ADVICE AND COMMUNICATIONS SPECIALIST/TILBURG, NETHERLANDS/5 MONTHS CONTRACT/42 TO 65 EUR (PER HOUR)

THE ROLE

The role of a Medical Advisor (MA) is to be a therapeutic area scientific expert, responsible for discussing our products, patient treatment trends and studies in the therapeutic areas in which we are involved, on a peer-to-peer basis with a defined audience of external clinical and non-clinical stakeholders (Physicians, Pharmacists, Hospital Managers, Board Members of Scientific Societies, and other stakeholders) to feed and adjust, if needed, the overall stakeholder mapping and Cluster Value Team (CVT) strategy.

An MA is to be considered a trusted scientific counterpart and partner.

The MA is responsible for translating the CVT strategy into country specific tactics and tools and implementing them together with the Medical Scientific Liaison (MSL) within the assigned therapeutic area (TA).

The MA is responsible for translating, processing and providing medical field' info, study info and other country-specific info towards the Medical Affairs Manager (MAM)/CVT.

THE COMPANY

Johnson & Johnson is an American multinational medical devices, pharmaceutical and consumer packaged goods manufacturer founded in 1886.

PROFILE/QUALIFICATIONS

- Scientific degree: Medical Doctor, pharmaceutical or other biomedical degree
- Minimal 3-5 years within Medical Affairs in the pharmaceutical industry or equal relevant experience
- Deep knowledge of the therapeutic area, strength in research and interpretation of medical data
- Strategic thinking to promote growth, process improvement and gaining competitive advantage
- Excellent analytical, communication, and presentation skills for interaction with external and internal customers and partners
- Able to work in a team and independently: show leadership, influencing and negotiation skills
- Business acumen: Understanding of business administration and translation into tactical plans and tools
- High customer focus with an understanding of the importance of business results and be able to apply problem-solving strategies
- Innovative, able to work in a Matrix and coordinate and drive a complex and changing environment
- Being persistent and willing to make tough decisions
- Awareness of, and adherence to, Johnson & Johnson Credo values and International Health Care Business Integrity Guidelines
- Willing to comply with regulatory requirements and with company policy on business integrity
- Languages: Dutch, preferably French (when working in Belgium), English: spoken, written
- Computer skills: knowledge of Microsoft Office (Email, PowerPoint and Excel) and using new technologies to improve health care delivery

TASKS AND RESPONSIBILITIES

The function Medical Advisor contains the following main tasks & responsibilities:

- To keep abreast of medical and scientific knowledge
- Continuously update his/her knowledge of products, patient treatment trends and clinical activities and studies within the therapeutic area and patient treatment trends in the region
- Identify evolving scientific concepts with future clinical implications
- Be a TA scientific expert, considered and recognized as a trusted scientific counterpart and a partner
- Development and maintenance of a contact network with external stakeholders
- Understand their needs, key value drivers, practical treatment patterns and scientific activities within the therapeutic area
- Develop and monitor operational excellence of the stakeholder plan
- Develop and execute medical excellence and medical leadership in his/her assigned TA for the local market
- Develop and maintain a contact network with a small group of targeted stakeholders for assigned country
- Develop a company country vision on treatment paradigms/patient treatment trends/studies in the TA
- Proactive and reactive communication of medical scientific data to external stakeholders:
- Communicate non-promotional general information about our company, including pipeline, research and development programs and other relevant information
- Use digital technologies and new media to support proactive and reactive communication
- Planning and/or organization and/or participation in Advisory Boards in cooperation with the Medical Scientific Liaison/Medical Affairs Manager
- Provision of scientific support to internal company stakeholders
- Act as a reference point for internal company stakeholders for any scientific query, in collaboration with Medical Information as appropriate
- Develop and execute Medical Affairs (MAF) plan as part of the CVT plan
- Provide medical input into CVT and align with brand planning & strategy
- Be an ad hoc member of the CVT by contributing to the medical leadership of the MAM by providing local insights of the assigned country market
- Align and optimize CVT strategy and medical tactics through regular communication with the Medical Science Liaison (MSL) & MAM
- Translate MAF plan into country-specific tactics, in line with CVT plan, together with MSLs
- Manage MAF budget for assigned country
- Accountable for Medical Affairs evidence-generating activities, planning, design and execution in close co-operation with Global Clinical Operations (GCO) and external service provider (ESP).
- Support the setting up and follow-up of registries and other non-interventional Medical Affairs studies
- Identify the need for and then set up a pre-approval access program within the legal boundaries
- Profound knowledge of Real World Evidence (RWE) methodologies, identify data needs, gaps and opportunities. Support protocol development and engage in discussions with customers to help design RWE projects in line with CVT strategy and in close collaboration with RWE lead
- Propose investigators and sites for interventional and non-interventional Medical Affairs studies
- Support GCO and ESPs in site set-up, management and issue resolution
- Contribute to preparation and conduct of investigator meetings, recruitment follow-up and presentation of study results
- Plan investigator meetings, develop patient recruitment strategies with GCO, follow-up of study/results/presentations/publications
- Receive and manage investigator proposals for investigator-initiated studies and ensure they are discussed within the Medical Affairs department for decision
- Support post-marketing surveillance and early access programs/compassionate use/medical need programs
- Role of Study Responsible Physician/Scientist where needed/applicable
- Through scientific interactions, gain valuable insights into treatment patterns, and scientific activities in the therapeutic area and provide strategic input to the company Medical Affairs Plan/business decision-making.
- Through scientific interactions with a predefined group of external stakeholders, in line with the stakeholder plan, increases the medical value of our products fairly, based on the risk-benefit profile of our drugs and contributes to fostering innovative therapeutic approaches to benefit patients.
- Ensure compliance
- Make sure all activities deployed are in line with Health Care Business Integrity regulations and local and EMEA standard operating procedures and ensure review by the Medical Affairs Manager (and Health Care Compliance in case of value transfer).

If you match these requirements, please apply in the normal way. Elevate will send you an email, please open, click and action that email and your application will be visible to the hiring organisation directly.

Projektdetails

  • Einsatzort:

    Tilburg, Niederlande

  • Projektbeginn:

    asap

  • Projektdauer:

    5 months

  • Vertragsart:

    Contract

  • Berufserfahrung:

    Keine Angabe

Geforderte Qualifikationen

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