Roche Posted August 3, 2026

Medical Value Partner Tunisia & Libya

Tunis, Tunisia Full time
Medical Affairs

Roche is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

At Roche you can show up as yourself, embraced for the unique qualities you bring. Our culture encourages personal expression, open dialogue, and genuine connections,  where you are valued, accepted and respected for who you are, allowing you to thrive both personally and professionally. This is how we aim to prevent, stop and cure diseases and ensure everyone has access to healthcare today and for generations to come. Join Roche, where every voice matters.

The Position

The Medical Value Partner is a key strategic leadership role requiring therapeutic area expertise and clear business understanding to identify and address the relevant medical needs in clinical practice to successfully support the optimal use of Roche products.

Linking the affiliate with the global medical affairs objectives to deliver on data generation, knowledge exchange/ data communication, and to lead Therapeutic Areas Experts engagement and development in a scientific manner.

Providing high caliber medical support to internal partners (Primary Points of Contact (PPOC: Patient Journey Partner “PJP” and Healthcare System Partner “HSP”), Regulatory) on scientific and medical issues to achieve the affiliate objectives.

Acting as a guardian for high standards of compliance, ethics and safety of Roche products, while putting the patient at the center of every action.

Leading specific transverse and strategic projects within the Innovation and Partnerships chapter

Ensuring all medical information enquiries from customers are answered in a balanced, accurate, ethical and timely manner

Supporting the safe and effective use of Roche products

Primary Responsibilities and Accountabilities

Medical Strategy and Planning:

Identify unmet medical needs at medical and scientific customer sites

Identify key medical knowledge gaps and propose appropriate action plan

Develop Medical strategy, projects & tactics in the concerned therapeutic area to address questions and concerns from the scientific community

Develop clinical messages for the product line to support achieving the affiliate objectives

Lead the scientific affairs team to achieve the plan

Lead the pre-launch activities

Manage the budget

Implement tools to monitor the medical activities

Attend appropriate regional and international scientific congresses

TAE interactions & development:

Responsible for setting up and follow up of 1 to 1 meeting and Advisory Boards to collect input on disease areas, treatment algorithms, clinical data, unmet medical needs, protocol design, and medical education needs.

Maintain, strengthen, and develop sustainable partnership with KOLs/ Scientific Associations

Coordinate and follow up of the Medical insights collection related to the medical strategy.

Responsible for presenting medical content: pipeline and medical educational content

Compliance:

Make sure all service activities and behavior in business are in compliance to Roche standards and guidelines (Symphony, SOPs, and code of conduct)

Clinical Operations:

Plan, design, Oversight of execution and report of clinical trials according to ICH-GCP, Roche SOPs and local regulation.

Identify opportunities to engage Roche Tunisia in local Investigator Initiated Studies

Development of effective interactions with clinical Operations including but not limited to placing studies, provide input on feasibility, sites and investigator selection.

Internally:

Work cross-functionally with internal functions to ensure strategic alignment and in Global squads as needed

Act as the medical expert in disease and product by detecting, analyzing and sharing new data about the portfolio products and competitive assets with Disease Area Team

Support regulatory and healthcare system shaping to achieve timely products registration and access

Approval of promotional materials, and external medical content in accordance with Roche SOPs

Support the Pharmacovigilance and Medical Information Responsible

Medical Projects:

Lead strategic Projects within the affiliate to accelerate switch to innovation

Medical information:

Ensuring all medical information enquiries from customers are answered in a balanced, accurate, ethical and timely manner

Supporting the safe and effective use of Roche products

Ensure that all enquiries related to designated Roche Products received from all sources (e.g. via phone; e-mail; letter; fax; face to face) are resolved to the required standard.

Respond or triage all unsolicited enquiries from customers on Roche products, including both on and off-label enquiries.

Ensure they provide scientific, balanced and up to date information on Roche products to external and internal customers.

Ensure responses are timely, meeting local requirements

Identify, collecting and reporting any AE and/or other reportable event and forward to drug safety department within timelines described in relevant SOPs

Identify and reporting any product quality complaint and forward to local complaint manager within timelines described in relevant SOPs.

Ensure integrity and scientific accuracy of the MI responses if applicable.

Ensure copyright compliance for documents provided to the customer if applicable.

Professional and Technical Requirements

Education/Qualifications:

Medical degree/Scientific background

Business administration and Project management training is a plus

Experience, Knowledge & Competencies

Experience

Professional experience within pharmaceutical industry desirable but not mandatory

Experience and knowledge of oncology therapeutic area is preferable

Knowledge of the overall drug development process relevant to pharmaceutical/ biothechnology organizations

Experience in development and implementation of clinical trials

Experience in the principles and techniques of data analysis, interpretation and clinical relevance

Experience of writing clinical publications and delivery of scientific presentations

Relationships with external TAEs, and external organization is strongly preferred

Experience in working with senior business leaders, clinicians and regulatory authorities

Knowledge:

ICH,GCP and local regulations

Appreciate the diversity of working with multifunction teams

Knowledge of drug discovery & commercialization process

MS office literate

Fluent English language knowledge, written and verbal

Competencies:

Strategic thinking

Leadership skills

Analytical skills

Results orientation

Communication, interpersonal and networking skills

Negotiation skills

Presentation skills

Knowledge in data analysis and statistics

Mindset:

Strong organization skills

Good communication skills

Good time and priority management

Strong team player

Open-minded and flexible

Customer service orientated

Entrepreneurial spirit with strong partnership skills

Growth mindset, coaching, active listening

Ability to learn and self-challenge quickly, take risks and experiment, and contribute to the learning cycle by sharing knowledge with others inside and outside

Autonomous and altruistic in supporting the global network

High sense of integrity in everything he/she does (ie open, honest, ethical and authentic)

Facilitator leveraging internal and external networks to create value, share and scale

 

 

Who we are

A healthier future drives us to innovate. Together, more than 100’000 employees across the globe are dedicated to advance science, ensuring everyone has access to healthcare today and for generations to come. Our efforts result in more than 26 million people treated with our medicines and over 30 billion tests conducted using our Diagnostics products. We empower each other to explore new possibilities, foster creativity, and keep our ambitions high, so we can deliver life-changing healthcare solutions that make a global impact.

Let’s build a healthier future, together.

Roche is an Equal Opportunity Employer.

Job details

Seniority
Not listed
Function
Medical Affairs
Therapeutic area
Not listed
Location
Tunis, Tunisia
Employment type
Full time

How this role compares

Computed from every other active Medical Affairs role in our database, not just this employer's listings.

We currently track 924 comparable Medical Affairs roles across 130 biopharma companies.

924Comparable roles tracked
799Currently active
130Companies hiring similar roles
57Countries represented

Salary context

175 of 924 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Lowest disclosed · Clinical Coordinator · Pfizer $79,400/yr – $132,400/yr
Peer group range $105,900 – $458,800 (median $232,750)

Where these roles are based

Top locations among the 924 comparable roles

United States379
China's Mainland69
Japan61
China57
India50
Germany40

+ 51 more countries

Seniority mix

502 of 924 peers have a known seniority level

Director148
Manager125
Senior97
Associate55
Associate Director39
Senior Director20
Executive/VP11
Principal5
Intern/Fellow/Postdoc2

Therapeutic area mix

326 of 924 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology114
Immunology52
Neuroscience35
Cardiovascular / CVRM34
Respiratory21
Vaccines & Infectious Disease21
Rare Disease21
Dermatology & Aesthetics20
Ophthalmology4
Gastroenterology4

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

25%similar
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25%similar
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How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

25%
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AstraZeneca · Minato-ku, Tokyo, Japan · Director
Function Therapeutic area Seniority Country
25%
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Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.