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Theratechnologies Inc T.TH

Alternate Symbol(s):  THTX

Theratechnologies Inc. is a Canada-based clinical-stage biopharmaceutical company. The Company is focused on the development and commercialization of therapies addressing unmet medical needs. It markets prescription products for people with human immunodeficiency viruses (HIV) in the United States. The Company's research pipeline focuses on specialized therapies addressing unmet medical needs in HIV, nonalcoholic steatohepatitis (NASH) and oncology. Its medicines include Trogarzo and EGRIFTA SV (tesamorelin for injection). Trogarzo (ibalizumab-uiyk) injection is a long-acting monoclonal antibody which binds to domain 2 of the CD4 T cell receptors. It blocks viral entry into host cells while preserving normal immunologic function. The Company is also investigating an intramuscular method of administration of Trogarzo. EGRIFTA SV (tesamorelin for injection) is approved in the United States for the reduction of excess abdominal fat in people with HIV who have lipodystrophy.


TSX:TH - Post by User

Post by scarlet1967on Aug 22, 2021 2:41pm
210 Views
Post# 33746348

Recruiting

Recruiting As July 9 the below was list of jobs advertised on the company's LinkedIn account. The list is down to two positions now. Their website however has more postings but I believe they don't update the carrier section regularly as I have seen job offering disappear on LinkedIn account and sometimes weeks later they are taken down on the website.
It seems they have been recruiting aggressively recently.

Clinical Supply Manager

Position Summary

 

The incumbent will be responsible for establishing and managing all the supply chain related activities for the clinical projects at Theratechnologies Inc. 

Key Responsibilities

Planning the manufacturing (including required quantities to fill requests from clinical team) to ensure continuity of clinical supplies

Monitor inventories

Manage logistics for product shipments from CMO’s to clinical distributor

Manage clinical distributor (shipment to clinical sites)

Manage logistics/shipments for clinical test kits from testing labs to clinical sites

Manage logistics/shipments of clinical samples (e.g blood and biopsies) from clinical sites to testing labs

Monitor budget for all the above, take care of contracts, POs, invoice approvals, change orders, etc.

Develop and/or procure clinical secondary and tertiary packaging (e.g. carton for vials, and shipper boxes) and ensure adequacy for given shipment conditions (e.g. dry ice)

Determine permit requirements, perform permit application/renewal and maintain valid permit or ensure that CMO has valid permit at all time

Manage  EU importation and release for distribution

Develop and implement contracts with an EU warehouse/clinical distributor

Performs any other duties required by the management

External Customers

CMO’s

TPL’s

Analytical Laboratories

 

Preclinical Project Manager | Chef de projets prcliniques

 

The incumbent is responsible for the liaison and coordination as well as providing scientific support to internal and external partners in terms of international preclinical projects management, including follow-ups. The incumbent also has to ensure that related timelines and budgets are met, activities are properly executed, and adequate resources are allocated.

Key responsibilities

Planning and managing preclinical projects for different programs

Plan preclinical projects and contribute to their budget elaboration, resource allocation, and update timelines as required, with the contribution from team members

Participate in the selection and qualification of external suppliers, and in the execution of related agreements (e.g. services agreement, quality agreement, data transfer)

Approve monitoring plan for external suppliers and performance requirements

Plan and anticipate upcoming difficulties in plan execution, prepare contingency plans and strategies to overcome these difficulties

Activities Execution 

Perform follow-ups and supervision related to assigned preclinical projects with internal and external partners

Provide technical/scientific support to internal and external partners

Review literature associated with development of preclinical projects

Stay informed of regulatory procedures, guidance documents, standards, and changes in regulatory and quality environment for preclinical studies

Prepare scientific and non-scientific documentation required to execute preclinical projects

Review and approve documents related to preclinical projects such as instructions, methods, protocols, and reports

Participate in the preparation and revision of standard operating procedures (SOPs) and to the change control process

Prepare and present progress report and tables or diagrams of projects (e.g. Gantt Chart, presentations)

Prepare and chair preclinical project meetings, and write meeting minutes

Approve expenses for activities under his/her responsibility

Assume Project Ownership

Ensure that projects are running smoothly

Follow-Up on timelines with other team members

Discuss encountered difficulties with team members and/or management, and obtain support as required

Discuss performance deficiencies with team members, and if required, with supervisor

Perform other tasks and activities as required by management

External customers

External partners or service providers involved in preclinical projects such as academic laboratories, research institutions, analytical or bio-analytical testing laboratories, contract research organizations (CROs), consultants, warehouses, transporters, etc.

 

Gestionnaire ou Directeur mondial, tablissement des prix et du remboursement | Manager or Director, Global Pricing & Reimbursement

 

Position Summary

Reporting to the Global Commercial Officer, the Global Pricing & Reimbursement Lead will play a critical leadership role in developing, leading and coordinating plans and related core deliverables aimed at building, shaping and expanding access and securing reimbursement for Theratechnologies current and future products in HIV, oncology, and hepatology (NASH).  

Key Responsibilities

Responsible for Global payer strategic planning to support value and access optimization for Theratechnologies portfolio

Provide immediate support and strategic direction to optimize pricing and expand the reimbursement of products in Europe and other international markets.

Evaluate the current market access resources and practices at Theratechnologies and recommend a fit for purpose model to support imminent needs and mid-longer-term growth aspirations.

Advise company leadership regarding market access, reimbursement, value assessment framework, health policy trends or matters, and competitive intelligence that may impact Theratechnologies market access efforts (monitoring, horizon scanning)

Increase corporate visibility and build alliances with key stakeholders to support the successful reimbursement of Oncology and NASH launch assets in priority countries.

Collaborate closely with medical, regulatory, and commercial experts to anticipate the timing and conditions of market access for the in-line and pipeline products.

Lead the development of market access strategy which integrates value evidence generation, strategic pricing, stakeholder engagement to support successful reimbursement and pricing

Identify and partner with strategic partners (outside consultants) to achieve optimal outcomes for reimbursement and pricing strategies and local implementation

Bring an understanding of the payer perspective to the cross-functional teams to ensure that payer requirements are adequately addressed throughout the clinical and commercial development processes.

Identify the need for and oversee the development of health economics and outcomes studies to support a compelling and credible value proposition for payers

Nurture relationships with KOLs and Patient Advocacy Groups on issues related to access and health policy arena and represent the company at various access forums

Monitor and report on Theratechnologies progress against set market access objectives by using a well-defined tracking system (score card, metrics).

Overtime, build and lead a high performing and efficient market access team to support the successful launch and ongoing commercialization of Theratechnologies products.

Internal clients

Global commercial officer and team, Chief Medical Officer and team, Market Access hub, therapeutic area team, Corporate Affairs, Legal, General Manager Europe.

External clients

Health authorities (HTA, public and private payers), policy makers, government officials, advocacy groups, academia, NGOs.

Communications Manager

 

Description

The Manager, Communications is responsible to implement the Company’s overall communication strategy, in Canada, the United States and Europe, to enhance its corporate profile, support investor relations and interact with sales and marketing as required to support the business and strategic objectives of the Company by building its corporate branding, notoriety and reputation.

The position is based in Montreal, Canada and reports to the Vice President, Communications and Corporate Affairs.

Responsibilities

Assist the VP, Communications and Corporate Affairs in the development and implementation of communication strategies in Canada, the United States and Europe to protect and enhance Theratechnologies reputation and support business objectives

Develop and implement Corporate Social Responsibility plan

Drive coverage across a broad range of media, including social, broadcast, print, specialized and consumer outlets

Increase social media impact

Help to attract and retain employees through internal communications

Help generate public speaking opportunities for the CEO

Update and upgrade corporate website as needed

Translation English to French of press releases and other related documents

Manage patient engagement/awareness campaigns with patient associations

Manage external agencies as required

Interact with all divisions of the Company including Medical, Sales and Marketing

Handle media enquiries

Organize events

Prepare briefing materials and brief executive spokespeople

 

Conseiller(re) mdical(e) principal(e), NASH/Senior Medical Advisor, NASH

 

Your Role

As the Senior Medical Advisor, you will be responsible for the scientific integrity of the clinical program and the translation of scientific information into business concepts, as well as the validation of scientific concepts and production product advocacy. You will also support the Medical Advisory Manager in the elaboration of abstracts and manuscripts for publication.

This is how your days will look like

Interact with medical and scientific experts to validate scientific concepts and create

advocacy

Lead the preparation of the scientific rationale and design of study protocol

Follow patient safety parameters throughout the study and answer scientific and medical

from study sites, liaising with medical director as appropriate

Research protocol-specific technologies

Lead the analysis and interpretation of study results and the creation of the final study

Write abstracts and manuscripts for publication

Critically review scientific literature and disseminate relevant information

Review the scientific accuracy of corporate materials for external use

Prepare scientific documents, as required

Manage the Medical Writer under your responsibility

Lead key cross-functional initiatives relating to Regulatory submissions

Act as an internal scientific resource for junior team members

 

Gestionnaire ou Directeur mondial, tablissement des prix et du remboursement | Manager or Director, Global Pricing & Reimbursement

 

Key Responsibilities

Responsible for Global payer strategic planning to support value and access optimization for Theratechnologies portfolio

Provide immediate support and strategic direction to optimize pricing and expand the reimbursement of products in Europe and other international markets.

Evaluate the current market access resources and practices at Theratechnologies and recommend a fit for purpose model to support imminent needs and mid-longer-term growth aspirations.

Advise company leadership regarding market access, reimbursement, value assessment framework, health policy trends or matters, and competitive intelligence that may impact Theratechnologies market access efforts (monitoring, horizon scanning)

Increase corporate visibility and build alliances with key stakeholders to support the successful reimbursement of Oncology and NASH launch assets in priority countries.

Collaborate closely with medical, regulatory, and commercial experts to anticipate the timing and conditions of market access for the in-line and pipeline products.

Lead the development of market access strategy which integrates value evidence generation, strategic pricing, stakeholder engagement to support successful reimbursement and pricing

Identify and partner with strategic partners (outside consultants) to achieve optimal outcomes for reimbursement and pricing strategies and local implementation

Bring an understanding of the payer perspective to the cross-functional teams to ensure that payer requirements are adequately addressed throughout the clinical and commercial development processes.

Identify the need for and oversee the development of health economics and outcomes studies to support a compelling and credible value proposition for payers

Nurture relationships with KOLs and Patient Advocacy Groups on issues related to access and health policy arena and represent the company at various access forums

Monitor and report on Theratechnologies progress against set market access objectives by using a well-defined tracking system (score card, metrics).

Overtime, build and lead a high performing and efficient market access team to support the successful launch and ongoing commercialization of Theratechnologies products.

Internal clients

Global commercial officer and team, Chief Medical Officer and team, Market Access hub, therapeutic area team, Corporate Affairs, Legal, General Manager Europe.

External clients

Health authorities (HTA, public and private payers), policy makers, government officials, advocacy groups, academia, NGOs.

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