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Small Biotech Company Jobs (NOW HIRING)

Tango Therapeutics

Clinical Contract Manager

Boston, MA · On-site

$128K - $193K/yr

Company Overview Tango Therapeutics is a biotechnology company dedicated to discovering novel drug ... In a fast-paced, small biotech environment, the CCM will drive the development, negotiation ...

Tango Therapeutics

Clinical Trials Manager

Boston, MA

Company Overview Tango Therapeutics is a biotechnology company dedicated to discovering novel drug ... In a fast-paced, small biotech environment, the CTM will operationally manage the set-up, conduct ...

Tango Therapeutics

Clinical Trial Leader

Boston, MA · On-site

$160K - $241K/yr

Company Overview Tango Therapeutics is a biotechnology company dedicated to discovering novel drug ... In a fast-paced, small biotech environment, the CTL will operationally lead the set-up, conduct and ...

Tango Therapeutics

Clinical Supply Manager

Boston, MA · On-site

$131K - $196K/yr

Company Overview Tango Therapeutics is a biotechnology company dedicated to discovering novel drug ... In a fast-paced, small biotech environment, the CSM will plan, execute and oversee clinical ...

Tango Therapeutics

Clinical Trials Manager

Boston, MA · On-site

Company Overview Tango Therapeutics is a biotechnology company dedicated to discovering novel drug ... In a fast-paced, small biotech environment, the CTM will operationally manage the set-up, conduct ...

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How much do small biotech company jobs pay per hour?

As of Jun 14, 2026, the average hourly pay for small biotech company in the United States is $22.08, according to ZipRecruiter salary data. Most workers in this role earn between $18.03 and $24.52 per hour, depending on experience, location, and employer.

What is the difference between Small Biotech Company vs Research Associate?

AspectSmall Biotech CompanyResearch Associate
Required CredentialsBachelor's or Master's in Life SciencesBachelor's or Master's in Life Sciences
Work EnvironmentFast-paced, startup-like setting with cross-functional teamsLaboratory-focused, often in academic or industry labs
Employer & Industry UsageBiotech startups, small biotech firmsResearch institutions, biotech companies, pharmaceutical firms
Common Search & ComparisonOften compared for entry-level roles in biotechCommonly compared for laboratory technician or research roles

Small Biotech Companies and Research Associates typically require similar educational backgrounds and work in laboratory or research settings. While Small Biotech Companies are characterized by dynamic, startup environments, Research Associates often work within established labs. Both roles are essential in biotech and research industries, with the main differences lying in company size and work setting.

What are the key skills and qualifications needed to thrive as a professional in a small biotech company, and why are they important?

Working in a small biotech company requires a strong background in biological sciences or related fields, often with advanced degrees and hands-on laboratory experience. Familiarity with lab equipment, data analysis software, and regulatory compliance systems like GLP or GMP is typically expected. Adaptability, problem-solving, and effective collaboration are vital soft skills due to the dynamic and multidisciplinary nature of small teams. These skills and qualities enable individuals to contribute flexibly, innovate quickly, and drive the company's scientific and business goals forward.

What is a small biotech company?

A small biotech company is a business that focuses on developing products and technologies using biological systems, living organisms, or their derivatives, and typically has a limited number of employees and resources compared to larger pharmaceutical or biotech firms. These companies often specialize in areas such as drug development, diagnostics, or agricultural biotechnology, and may work on innovative solutions or therapies. Small biotech companies are known for their agility and ability to pursue cutting-edge research, but they may face challenges in funding, regulatory approval, and commercialization. Many seek partnerships or investments from larger companies to advance their projects.

What unique challenges might I face working at a small biotech company compared to larger organizations?

Working at a small biotech company often means you'll wear multiple hats and handle a broader range of responsibilities than you might at a larger firm. Resources—such as funding, equipment, and support staff—can be more limited, so adaptability and problem-solving skills are essential. However, you'll likely enjoy greater visibility, closer collaboration with leadership, and more direct impact on the company's success. This environment can accelerate learning and provide unique opportunities for career growth, but it may also involve navigating uncertainty and frequent changes in priorities.
More about Small Biotech Company jobs
What job categories do people searching Small Biotech Company jobs look for? The top searched job categories for Small Biotech Company jobs are:
Small Biotech Company jobs near you
Infographic showing various Small Biotech Company job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 76% Full Time, 20% Part Time, and 3% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $45,925 per year, or $22.1 per hour.
Clinical Contract Manager

Clinical Contract Manager

Tango Therapeutics

Boston, MA • On-site

$128K - $193K/yr

Full-time

Posted 7 days ago

Job description

Company Overview
Tango Therapeutics is a biotechnology company dedicated to discovering novel drug targets and delivering the next generation of precision medicine for the treatment of cancer.
Using an approach that starts and ends with patients, Tango leverages the genetic principle of synthetic lethality to discover and develop therapies that take aim at critical targets in cancer.
This includes expanding the universe of precision oncology targets into novel areas such as tumor suppressor gene loss and their contribution to the ability of cancer cells to evade immune cell killing.
The Tango labs and offices are located at 201 Brookline Avenue, in the Fenway area of Boston, Massachusetts.
Summary
We are seeking a Clinical Contract Manager (CCM) to lead the end-to-end clinical site contracting process in support of our growing clinical portfolio. This role will serve as the primary sponsor contact for Contract Research Organization (CRO) partners and internal stakeholders across Clinical, Legal, Finance, and Compliance.
In a fast-paced, small biotech environment, the CCM will drive the development, negotiation, execution, and maintenance of Clinical Trial Agreements (CTAs), ensuring alignment with trial timelines, budget, and regulatory requirements. This individual will play a key role in enabling timely site activation, CTA maintenance as per trial requirements, proactively identifying and mitigating risks, and ensuring compliance of CTAs with applicable regulations and internal standards.
The ideal candidate is highly collaborative, detail-oriented, and comfortable operating in a hands-on environment, with a focus on building scalable processes, tools, and best practices to support efficient and compliant clinical trial execution.
Your Role
  • Serve as Sponsor key contact for CRO functions involved in Clinical Trial Agreement (CTA) development, negotiation, execution and maintenance.
  • Facilitate communication and collaboration between internal and external contributors (e.g., Legal, GDPR, Finance, Clinical Trial Team (CTT) members).
  • Organize and coordinate meetings with key stakeholders, including decision tracking and action item follow-up.
  • Contribute to development of templates, training material, and playbook.
  • Develop site contracting plan in line with approved budget and fair market value.
  • Align with Clinical Trial Leader (CTL)/ Clinical Trial Manager (CTM) and/or Site Management Leader (SML) on site activation plan and priorities.
  • Oversee and track end-to-end CTA workflow and report progress to CTL/ CTM and/or SML.
  • Identify risks and issues related to contracting plan and lead the development and implementation of mitigation strategies and action plans.
  • Manage CTA review and approval by internal contributors (e.g., Legal, CTL).
  • Manage accurate and up-to-date CTA information in systems and communication tools.
  • Train external contributors (e.g., CRO functions involved in CTA process).
  • Participate in CTT meetings and CRO meetings, as needed.
  • Keep Sponsor Legal informed of site activation plan and priorities.
  • Ensure CTA compliance with applicable regulations (e.g., SOX compliance, Sunshine Act, and Fair Market Value).
  • Support investigator budget forecasting, accrual processes, and reconciliation.
  • Ensure ongoing inspection and audit readiness of CTAs; participate in internal audits and regulatory inspections, as required.

What You Bring
  • 5+ years of trial management experience with 3+ years in site management.
  • Bachelor's degree in Life Sciences, Pharmacy or related field.
  • Experience working in global clinical development organization.
  • Experience in Oncology development (preferred).
  • Direct experience with site health authority inspections (FDA, EMA, MHRA, etc.) incl. sponsor GCP inspections (preferred).
  • Experience in outsourcing and oversight.
  • Familiarity with clinical trial systems (e.g., CTMS, eTMF) and operational metrics, KPIs, and KRIs.
  • Familiarity with site contracting requirements and healthcare compliance (Fair Market Value, SOX Act, Sunshine Act)
  • Knowledge in ICH-GCP, FDA guidelines, EU CTR and other relevant guidelines.

#LI-Hybrid
We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status
Salary range
$128,800-$193,200 USD

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