Senior Counsel

United States

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Not SpecifiedCompensation

Expert & Leadership (9+ years)Experience Level

Full TimeJob Type

UnknownVisa

Life Sciences, Pharmaceuticals, Clinical TrialsIndustries

Requirements

Candidates must possess a JD degree from an accredited law school with excellent academic credentials and be a member of the Bar in their state of residence. A minimum of 7-10 years of legal experience, either at a law firm or in-house at a healthcare technology company, is required, with a combination of experiences being a plus. Prior experience managing external counsel is also necessary. The ideal candidate will have superior analytical, problem-solving, and communication skills, exceptional attention to detail, and the ability to manage multiple matters in a dynamic environment. Knowledge of healthcare technology compliance requirements, strong interpersonal and customer service skills, and proven time management, priority management, planning, and coordination/multi-tasking abilities are essential. The candidate must also be able to maintain discretion and confidentiality.

Responsibilities

The Senior Counsel will advise and guide the Endpoint Clinical Executive Leadership Team on legal matters, developing legal strategies to protect and promote the company's interests. This role involves negotiating, structuring, and managing contractual documents such as Master Service Agreements, SaaS Agreements, Statement(s) of Work, Indemnity Agreements, Non-Disclosure Agreements, and Intellectual Property agreements. Responsibilities include maintaining a thorough knowledge of data rights and privacy implications (HIPAA, GDPR), advising on legal and regulatory requirements for clinical trials, and managing the IP portfolio. The Senior Counsel will also oversee the development and negotiation of contracts, maintain contracting postures, manage contracts staff, work with external counsel, and identify opportunities for efficiency and cost reduction, with a potential to grow into a full General Counsel role.

Skills

Contract Negotiation

Legal Strategy

SaaS Agreements

Master Service Agreements

Intellectual Property

Data Rights

HIPAA

GDPR

Compliance

Endpoint Clinical

Provides interactive response technology for clinical trials

About Endpoint Clinical

Endpoint Clinical provides interactive response technology (IRT) systems designed for clinical trials. Their systems assist with various trial processes such as managing drug supplies, randomizing patients, and scheduling visits. These systems are user-friendly and cater to clients in the life sciences sector, including pharmaceutical and biotechnology companies. Endpoint Clinical differentiates itself by focusing on ease of use and integration with other clinical trial management systems, ensuring that clients can streamline their processes and maintain regulatory compliance. The company's goal is to enhance the efficiency and transparency of clinical trials, allowing sponsors to conduct their research more effectively.

San Francisco, CaliforniaHeadquarters

2009Year Founded

$1.7MTotal Funding

DEBTCompany Stage

Enterprise Software, HealthcareIndustries

201-500Employees

Benefits

Remote Work Options

Risks

Emerging IRT providers with cost-effective solutions threaten Endpoint Clinical's market share.

Rapid AI advancements may outpace Endpoint Clinical's current technology offerings.

Decentralized trials could reduce demand for traditional IRT systems, impacting Endpoint's model.

Differentiation

Endpoint Clinical offers user-friendly IRT systems for clinical trial management.

The company specializes in drug supply management, patient randomization, and visit scheduling.

Endpoint Clinical collaborates with THREAD and Berlinger for integrated clinical trial solutions.

Upsides

Increased adoption of DCTs boosts demand for flexible IRT systems like Endpoint Clinical's.

AI integration in clinical trials offers Endpoint opportunities for advanced analytics.

Personalized medicine trends require sophisticated IRT solutions, benefiting Endpoint Clinical.

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