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Legal Counsel

Remote: 
Full Remote
Contract: 
Experience: 
Senior (5-10 years)
Work from: 
Alabama (USA), Colorado (USA), United States

Offer summary

Qualifications:

4-6 years experience in contract law, Experience with life sciences companies preferred, Master's degree in law preferred, In-depth knowledge of contracting processes, Experience with contracting tools and systems.

Key responsabilities:

  • Draft, negotiate, and review RD contracts
  • Serve as the subject matter expert for contracts
  • Collaborate with internal stakeholders on contracts
  • Ensure compliance with policies and best practices
  • Assist with other legal matters as needed
Stemline Therapeutics logo
Stemline Therapeutics Biotech: Biology + Technology SME https://www.stemline.com/
51 - 200 Employees
See more Stemline Therapeutics offers

Job description

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Your missions

Legal Counsel R&D

Reports to Assistant General Counsel (R&D and Clinical)


Opportunity


Stemline Therapeutics, Inc. is seeking a Legal Counsel (R&D) to join our growing legal team. The position will report to the Assistant General Counsel, R&D and Clinical. The primary role of the Legal Counsel (R&D) is to draft, review, and negotiate various types of contracts with clinical trial sites, consultants, vendors, research partners, and to implement processes, trainings, and systems related to managing these types of agreements, and to serve as the primary point of contact to the business for matters pertaining to these agreements. . We are looking for someone who enjoys working in a collaborative, team-oriented environment. The primary responsibility of this individual will be contracting, so experience drafting and negotiating biotechnology related agreements is highly preferred. The successful candidate is someone who is capable of working independently, exercises sound judgement and enjoys engaging with many different functions across the company.


Responsibilities


  • Drafting, negotiating, and reviewing contracts, particularly those related to R&D activities, including sponsored research and investigator-initiated studies, global clinical site contracts (CTAs, ancillary service agreements, MCTAs); informed consent forms; master service agreements and related statements of work with various R&D vendors; material transfer agreements; consulting agreements; confidentiality agreements; and research agreements.
  • Serving as the subject matter expert for outsourced and internal contracts professionals.
  • Reviewing documents to ensure adherence to Menarini Stemline policies, pharmaceutical industry requirements, compliance, and best practices.
  • Ensuring priorities are determined based on business needs and feedback.
  • Collaborating cross-functionally with internal stakeholders (such as Compliance, Privacy, Medical Affairs, Clinical Operations, and Clinical Development) to provide practical advice on potential business and legal risks of various contracts.
  • Coordinating with Finance and Procurement to ensure compliance with internal contracts approval procedures.
  • Possessing strong organisational and prioritization skills needed to manage multiple, parallel contracts processes and to work in a fast-paced, global environment.
  • Assisting, on an ad hoc basis, with other legal matters as they arise.
  • Contributing to ongoing process improvement and problem-solving by the legal department.

  • Skills/Knowledge


    • 4-6+ years’ experience working drafting and negotiating contracts
    • Experience with a life sciences company strongly preferred, but not required
    • Master’s degree in law, at a minimum; qualification preferred but not required
    • In-depth knowledge about contracting and procedures
    • Highly organised, detail-oriented, proactive, and strong follow-through skills
    • Experience with contracting tools and systems
    • Strong verbal and written communication skills in English
    • Strong problem solving and prioritisation skills, ability to take ownership of duties and lead various projects
    • Capability to work independently, without oversight
    • Pride in performance and its impact on Menarini Stemline’s success



    Menarini Stemline is an equal-opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees


    The Company


    Founded in 1886 in Naples under the name of Farmacia Internazionale, Menarini moved in 1915 to Florence where the Group’s headquarters are still located today. High quality therapeutics and diagnostics solutions for patients, ethics as our underlying principle, dedication to innovation and advancement, strong people centricity and environmental sustainability. These five pillars form the foundation of the Menarini Group, an Italian pharmaceutical company with nearly 135 years of history.


    The Menarini Group is present in 70 countries and our products are sold in 140 locations around the world. Its companies span from Europe to Asia, to Africa and the Middle East, to Central America and to the United States where with the acquisition of Stemline Therapeutics, a NASDAQ-listed biopharmaceutical company, the company marked its entry into the US oncology market.


    Thanks to the valuable contribution of around 18,000 employees, every year more than 500 million packs of drugs are produced at the Group's 18 manufacturing sites including a biotech plant for the manufacturing of monoclonal antibodies that also serves external clients distributed across 6 continents.


    Menarini has made a strong commitment to oncology, investing in a pipeline of five investigational compounds for the treatment of a variety of haematological and solid tumours. The acquisition of Stemline Therapeutics in June 2020, further strengthened Menarini’s oncology portfolio, adding both commercial and clinical-stage assets. Tagraxofusp is a novel, first in class targeted therapy for patients with blastic plasmacytoid dendritic cell neoplasm (BPDCN) and to date, the only approved treatment for BPDCN in the U.S. and EU, and the first and only approved CD123-targeted therapy. Tagraxofusp is also being evaluated as both a single agent and in combination, in other CD123+ indications, including acute myeloid leukaemia (AML), chronic myelomonocytic leukaemia (CMML), and myelofibrosis (MF).


    Additionally, Menarini received exclusive rights to commercialise Selinexor for the treatment of oncology indications in the European Union and other European countries (including the United Kingdom), Latin America and other key countries. Menarini has signed an exclusive licensing agreement with Karyopharm Therapeutics for the rights to commercialise an innovative therapeutic option in Europe, Latin America, Turkey, Russia, and CIS countries. Selinexor is a first-in-class, oral Selective Inhibitor of Nuclear export compound for the treatment of hematologic cancers and solid tumours. It is already marketed in the US for multiple myeloma and is under development for solid tumour indications. Selinexor is registered in the EU for both early and late lines.


    Menarini entered into a global licence agreement with Radius Health to complete the development of Elacestrant, an oral SERD in late-stage Phase 3 development for hormone receptor-positive advanced breast cancer. Following a successful phase 3 study, Menarini Stemline received FDA approval in January 2023 under priority review and successfully oversaw a strong launch in February to the US market with the EMA review process concluded positively in September 2023.


    Menarini’s commitment to oncology is also reflected in the investments made in the liquid biopsy diagnostic field through its affiliate Menarini Silicon Biosystems (MSB), a pioneer in rare cell analysis and non-invasive, advanced diagnostic solutions. MSB’s CELLSEARCH Circulating Tumour Cell (CTC) Test is the first and only clinically validated blood test cleared by the U.S. Food & Drug Administration (FDA) for detecting and counting CTCs in metastatic breast, prostate, and colorectal cancer when used in conjunction with other clinical monitoring methods.


    Since 2021, MSB has offered in the US a menu of non-invasive Laboratory Developed Tests (LDTs) provided through its CLIA/CAP accredited US-based Lab. The services include CMC enumeration, CTC enumeration and PDL-1/HER2 biomarker and offer a minimally invasive approach to follow cancer patient’s therapeutic journey.


    In 2022, the company launched the CELLSEARCH® Circulating Multiple Myeloma Cell (CMMC) Enumeration LDT, the first-of-its-kind, which directly measures levels of plasma cells in the blood of patients. This test provides new, complementary information to that of the bone marrow biopsy and other standard-of-care measures. Due to its minimally invasive nature, it can be performed serially to assess plasma cell burden without requiring repeated bone marrow biopsies.


    Menarini's vision and uniqueness in oncology is to bring together innovative therapeutic solutions and advanced liquid biopsy-based diagnostics for faster, more effective and precise patient management.


    It is an exciting time in the company’s development and an excellent opportunity for individuals joining us to contribute to building and shaping Menarini Stemline’s Oncology business.

  • Required profile

    Experience

    Level of experience: Senior (5-10 years)
    Industry :
    Biotech: Biology + Technology
    Spoken language(s):
    Check out the description to know which languages are mandatory.

    Soft Skills

    • Non-Verbal Communication
    • Detail Oriented
    • Problem Solving
    • Organizational Skills
    • Prioritization

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