Associate Counsel, Life Sciences - Technical.ly

Associate Counsel, Life Sciences

Certara

Remote Remote Only Sep 25
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Job Description

Overview

Certara accelerates the potential of bringing medicines to market and to patients using biosimulation software, technology, and services to transform traditional drug discovery and development. Our clients include more than 2,400 biopharmaceutical companies, academic institutions, and regulatory agencies across 70 countries.

Our goal is to enable the life sciences industry’s use of data, modeling, and analytics to make better decisions across the various phases of discovery and drug development. Our software and scientists incorporate modern advances in scientific understanding, drug development experience, data analysis, and AI resulting in significant opportunities to decrease the cost and increase the probability of success for new drug approval and commercialization.

Responsibilities

Responsibilities

We are seeking a commercially minded attorney to support our U.S. legal contracting function. You will negotiate a broad portfolio of life sciences and technology agreements, advise business teams in practical terms, and help deliver a disciplined, scalable contracting experience through clear templates, playbooks, and escalation standards.

You will have meaningful ownership of matters appropriate to your experience, with senior support for novel, high-risk, or strategically significant issues. Legal owns the contracting framework and legal terms. Commercial Operations continues to populate and execute order forms and task orders within Legal-approved templates.

  • Draft, review, and negotiate master services agreements, commercial and service agreements, SaaS and software license agreements, data privacy agreements and DPAs, vendor and consulting agreements, reseller agreements, development/developer agreements, and amendments, escalating novel or high-risk issues as appropriate.
  • Manage assigned matters from intake through signature, maintaining clear status, required approvals, and organized matter records.
  • Apply Legal playbooks, templates, approval thresholds, and fallback positions consistently; identify recurring issues that should be addressed through updated guidance, templates, or process improvements.
  • Advise business stakeholders in plain language and collaborate closely with Sales, Finance, Privacy, Security, Procurement, and Commercial Operations.
  • Review revisions that introduce legal or complex commercial terms, including revisions to evaluation agreements, and route matters for senior escalation when needed.
  • Support Legal ownership of order form and task order templates, including quality checks and controlled self-service.
  • Respect the operating boundary: Commercial Operations populates and executes order forms and task orders; Legal owns the framework, legal terms, templates, and escalations.
  • Contribute to knowledge management, training, metrics, template maintenance, playbook updates, and alternative legal talent/provider coordination.
  • Balance contract velocity and risk using sound judgment, strong organization, and responsive stakeholder communication.

Qualifications

• Juris Doctor (or equivalent law degree) and active membership in good standing in at least one U.S. jurisdiction.
• Approximately 1–3 years of relevant commercial transactions experience at a law firm, in-house legal department, or comparable environment.
• Strong foundational drafting and negotiation skills, particularly for MSAs, services agreements, SaaS/software licenses, SOW-related frameworks, and privacy/data-processing terms.
• Experience with life sciences, pharmaceutical, biotech, health technology, software, data, or professional-services transactions is strongly preferred.
• Working familiarity with privacy and regulated-data issues; exposure to HIPAA and GDPR is preferred.
• Sound judgment about when to resolve an issue independently and when to escalate.
• Strong organization, attention to detail, responsiveness, and comfort managing multiple matters and deadlines.
• Interest in contract playbooks, template maintenance, knowledge management, and process improvement.

How success will be measured

• Assigned agreements progress promptly, accurately, and in line with Legal playbooks and approval requirements.
• Escalations are timely and well framed, with clear facts, options, and recommended paths.
• Matter status, approvals, key dates, and supporting records remain accurate and complete.
• Templates and repeatable guidance are applied consistently, and recurring issues are surfaced for improvement.
• Business partners receive practical, clear, and responsive support.

Certara bases all employment-related decision on merit, taking into consideration qualifications, skills, achievement, and performance. We treat all applicants and employees without regard to personal characteristics such as race, color, ethnicity, religion, sex, sexual orientation, age, nationality, marital status, pregnancy, physical or mental condition, genetic information, military service, or other characteristic protected by law.

Employees at Certara do tech work that means something. Their software enables key transitions in the pharmaceutical development pipeline (from discovering new molecules, to predictively modeling their effects on humans, to actually conducting clinical trials) and streamlines regulatory approvals for drugs and medical devices, getting new treatments to patients faster.

Since Certara develops an integrated platform (“Certara Cloud”) and also offers multiple solutions or products tied to that platform, ideas and demand abound. What the company needs is more people to execute these ideas into reality: software engineers, data standards experts and product managers (and more!: software testers, clinical SMEs in PK/PD and TFL, support specialists, customer success, quality, etc) who can develop highly reliable products in the service of medicine.

With ~2,400 customer organizations across 66 countries, Certara has a truly global footprint, and is a leader in biosimulation, model-informed drug development and (increasingly) clinical trial data standardization and workflow automation.

Of Certara’s ~1,400 employees (430 of whom have Ph.D.s, Pharm.D.s, or M.D.s), and a track record of successfully acquiring 20+ complementary companies in the life sciences space, the team is large and growing. The company has proven a draw for technologists who prefer autonomy and thrive on the challenge of doing application development in a highly specialized scientific domain.  From what we heard in interviews with employees, it’s clear why. Certara, and its subsidiaries including Philly originals: Clingenuity, Synchrogenix, GlobalSubmit, and most recently Pinnacle 21, have made the list of Best Small & Medium Workplaces™ by Fortune and Great Place to Work®.

Certara respects the professionals who work there and recognizes their worth beyond the office walls. Generous PTO, flexibility when “life happens,” subsidized healthcare for the family, one-on-one career coaching — all stem from the company values. A brand new, spacious office in Radnor, PA, offers spaces indoors and out for breaks, snacks, coffee, workouts and games. Staff report how easy it is to decompress and enjoy the camaraderie of their “work fam.” If you’re looking for a new challenge in your career and work that creates tremendous impacts in the world of drug development, they’d love to hear from you!

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