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Rtsm Jobs (NOW HIRING)

Senior Manager, Vendor Management

OR ยท Remote

$150K - $163K/yr

Lead RFI/RFP processes, vendor evaluations, and bid defense meetings to select CROs, Labs, RTSM, electronic Clinical Outcome Assessments, Blood Pressure Monitoring and other various specialty vendors ...

Sr. Developer, AVP

NJ ยท On-site +1

$195K/yr

Conduct performance tuning by query optimization, tuning memory, and tuning disk usage with tools such as Explain Plan, RTSM, AWR, Hang Analyzer, ASH, and ADDM reports. * Facilitate Scrum sessions ...

Over 10 years of experience in Clinical Trials, Clinical Supply Chain, RTSM, or related fields. * Background in client relationship management, business development, or technical sales is highly ...

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Rtsm information

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$17K

$72.3K

$126K

How much do rtsm jobs pay per year?

As of Jul 15, 2026, the average yearly pay for rtsm in the United States is $72,301.00, according to ZipRecruiter salary data. Most workers in this role earn between $45,500.00 and $98,000.00 per year, depending on experience, location, and employer.

What is an RTSM job?

An RTSM (Randomization and Trial Supply Management) job involves managing clinical trial systems that handle patient randomization, drug assignment, and supply logistics. Professionals in this role ensure that trial participants receive the correct treatments while maintaining compliance with study protocols and regulations. They work closely with clinical operations, data management, and IT teams to configure and support RTSM software. Strong analytical skills and knowledge of clinical trial processes are essential for success in this role.

What are the key skills and qualifications needed to thrive in the Rtsm position, and why are they important?

To thrive as an RTSM (Randomization and Trial Supply Management) Specialist, you need expertise in clinical trial operations, data management, and a relevant bachelor's degree in life sciences or information technology. Familiarity with RTSM platforms (such as Medidata or Almac) and industry-standard certifications like GCP or IRT system training are highly beneficial. Strong attention to detail, problem-solving skills, and effective cross-functional communication are key soft skills in this position. These competencies are vital to ensure the accurate management of clinical trial supplies and randomization processes, maintaining regulatory compliance and supporting successful study outcomes.

What does a typical day look like for an RTSM Specialist in a clinical research organization?

A typical day for an RTSM Specialist involves overseeing clinical trial randomization processes, managing drug inventory, and addressing queries from clinical study teams to ensure the smooth operation of trial supply systems. You may participate in cross-functional meetings, troubleshoot IRT platform issues, and generate essential reports for project stakeholders. Collaboration with clinical operations, data management, and regulatory teams is common, as accuracy and timeliness in participant randomization and supply logistics are critical. This role often requires balancing multiple studies and adapting to shifting project timelines, making organizational and communication skills crucial for success.

More about Rtsm jobs
What states have the most Rtsm jobs? States with the most job openings for Rtsm jobs include:

Director, Clinical Technology Oversight Lead

BioNTech SE

Cambridge, MA โ€ข On-site

$168K - $268K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 6 days ago


Job description

Cambridge, US; Gaithersburg, US; New Jersey, US | full time | Job ID: 11055
About the Role:
As Director, Clinical Technology Oversight Lead at BioNTech, you will play a pivotal strategic leadership role in establishing and driving end-to-end governance, oversight and performance management of clinical technology vendors across our global clinical trial portfolio. Your work will ensure clear accountability, inspection readiness, and optimal vendor performance within an increasingly digital and AI-enabled ecosystem. By introducing a centralized governance framework, you will directly contribute to BioNTech's mission of revolutionizing medicine and advancing science to improve health worldwide.
Imagine yourself at the forefront of innovation, collaborating across departments such as Clinical Operations, Digital/IT, Procurement, and Quality Assurance to create scalable solutions that enhance trial delivery reliability and compliance. Your leadership will guide vendor performance and risk management while embedding cutting-edge AI governance frameworks into our processes.
Your Contribution:
  • Design and implement a global Clinical Technology Vendor Governance Framework aligned with ICH GCP E6 R3 and regulatory standards.
  • Oversee day-to-day vendor performance for technologies like EDC, eCOA, RTSM, eTMF, RBM, digital health solutions, and AI-driven systems.
  • Define KPIs, SLAs, and metrics tied to study timelines, data quality, system performance, and delivery reliability.
  • Establish robust AI governance frameworks ensuring transparency in intended use, decision boundaries, risk classification, validation processes, and lifecycle management.
  • Proactively manage risks through monitoring systems while maintaining inspection readiness for regulatory audits.
  • Serve as the central escalation point for issue resolution across internal teams and external vendors.
  • Drive strategic oversight of technology vendors to optimize scalability and cost-efficiency while fostering trust-based partnerships.

A Good Match:
  • Relevant degree in Vendor Management, Clinical Operations, Business Administration, Program Management or related discipline with12 years of clinical technology management experience with expertise in clinical trial technologies (EDC/eCOA/RTSM/eTMF/RBM/digital health) and AI/ML applications in trials.
  • Strong understanding of system architectures (APIs/data flows), cloud-based platforms (SaaS models), AI/ML fundamentals (bias/drift/validation), vendor oversight (SLAs/performance), and computerized system validation expectations.
  • Proven ability to translate complexity into clear governance structures while managing interdependencies across systems/processes.
  • Exceptional interpersonal skills with experience influencing stakeholders in matrix environments; fluency in English is required; German is advantageous.
  • Resilience in overcoming challenges coupled with agility to adapt to dynamic circumstances.

Your benefits and remuneration:
Expected Pay Range: $168,100/year to $268,700/year + benefits, annual bonus & equity (bonus and equity is variable and dependent on company and individual performance). Compensation for the role will depend on several factors, including responsibilities of the job, education, experience, knowledge, skills, and abilities.
BioNTech US is committed to employee wellbeing and offers best-in-class benefits & HR programs to support an inclusive & diverse workforce. Salaried/Position-Targeted Hourly Employees working 30+ hours per week are eligible for our comprehensive benefits package. Benefits include but are not limited to:
  • Medical, Dental and Vision Insurance
  • Life, AD&D, Critical Illness Insurance
  • Pre-tax HSA & FSA, DCRA Spending Accounts
  • Employee Assistance & Concierge Program (EAP) available 24/7
  • Parental and Childbirth Leave & Family Planning Assistance
  • Sitterstream: Virtual Tutoring & Childcare Membership
  • Paid Time Off: Vacation, Sick, Bereavement, Holidays (including Floating) & Year-End U.S. Shutdown.
  • 401(K) Plan with Company Match
  • Tuition Reimbursement & Student Loan Assistance Programs
  • Wellbeing Incentive Platforms & Incentives
  • Professional Development Programs
  • Commuting Allowance and subsidized parking
  • Discounted Home, Auto & Pet Insurance

...and more! More details to be shared.
Home to dozens of research institutions, biopharmaceutical companies, life science incubators, venture capital firms, and over 30 million square feet of laboratory space, Cambridge, Massachusetts has earned a reputation as the #1 life science cluster in the world. As part of the Greater Boston area, the city is often referred to as the "biotech supercluster" due to its high concentration of life sciences firms. This unique ecosystem is the result of a model partnership between academia and industry, fostering collaboration and innovation and driving the development of new therapies, medical devices, and diagnostics. As Cambridge's thriving life sciences industry continues to evolve, the city remains a beacon of knowledge, innovation, and collaboration, poised to shape the future of science and technology.
Apply now - We look forward to your application!
Apply for our Cambridge, US; Gaithersburg, US; New Jersey, US location and simply send us your documents using our online form.
By submitting your application, you acknowledge that a background check will be conducted as part of the recruitment process in accordance with applicable laws and regulations. If you are considered for the position, BioNTech will conduct the background check through our service provider 'HireRight'. You will be informed accordingly by your BioNTech-Recruiter.
Inspired? Become part of #TeamBioNTech.
BioNTech, the story
At BioNTech, we are more than just a biotechnology company - we are a community of innovators, scientists, and leaders dedicated to revolutionizing medicine by translating cutting-edge science into survival. Your contributions here have the potential to improve the health of people worldwide, especially by addressing diseases with high medical needs like cancer and various infectious diseases.
Experience a dynamic workplace that embraces diversity in all its forms. We foster innovation, encourage creativity, and develop business strategies driven by our shared passion for advancing medicine.
Working at BioNTech means striving to achieve medical breakthroughs while growing your career in a meaningful way. Apply today and become part of a mission that has the potential to change lives around the world.
BioNTech does not tolerate discrimination, favoritism or harassment based on gender, political views, religion or belief, nationality, ethnic or social origin, age, sexual orientation, marital status, disability, physical appearance, health status or any other physical or personal characteristics. BioNTech is committed to creating a diverse and inclusive work environment. We are proud to be an equal opportunity employer. The main thing is that you suit us, and we suit you!
BioNTech - As unique as you
www.biontech.com