- Company: Artbio
- Location: Cambridge, Massachusetts
- Salary: Pay not listed
Artbio at a glance
artbio.comSEC filings mentioning "Artbio": 13 — search EDGAR
3 employees covered under a retirement plan (2024 filing) — via DOL Form 5500 / EFAST2
Clinical trial sponsor: 2 trials registered, 1 currently active/recruiting — via ClinicalTrials.gov
Artbio (artbio.com) is the employer for this Senior Clinical Trial Manager role. Public DATA here is limited to the company domain; treat official site materials as the source of record for pipeline, sites, and team structure.
Senior Clinical Trial Manager at Artbio in Cambridge, Massachusetts - Full Time, No Remote
The Opportunity
The Senior Clinical Trial Manager will lead the day-to-day activities in a clinical trial and support the program strategy in a highly collaborative environment. This role involves managing members of the clinical operations team, including those at CROs and study vendors, working collaboratively with clinical trial sites, and partnering with key internal stakeholders to ensure clinical trial deliverables are completed on time, within budget, and in line with regulatory requirements.
Your Responsibilities
- Lead the day-to-day activities of a clinical trial
- Support program strategy in a collaborative environment
- Manage members of the clinical operations team, including CROs and study vendors
- Work collaboratively with clinical trial sites
- Partner with key internal stakeholders to ensure compliance and data quality
- Ensure clinical trial deliverables are completed on time, within budget, and in line with regulatory requirements
Qualifications
- Experience leading the day-to-day activities of a clinical trial
- Proven ability to manage members of the clinical operations team, including CROs and study vendors
- Ability to work collaboratively with clinical trial sites
- Strong partnership skills with key internal stakeholders
- Experience ensuring compliance and data quality in clinical trials
- Ambition to support program strategy in a collaborative environment
Why Join Artbio
At Artbio, you will have the opportunity to work on cutting-edge projects with a highly motivated team. Our culture is built around collaboration and innovation, providing a dynamic and supportive work environment.
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Explore Artbio online
Working in Cambridge, Cambridgeshire, UK
Weather right now in Cambridge, Cambridgeshire: checking… · Local time: · Air quality: · Daylight: · UV index: · Wind: · Pollen:
Cambridge is a city and non-metropolitan district in the county of Cambridgeshire, England. It is the county town of Cambridgeshire and is located on the River Cam, 55 miles (89 km) north of London. As of the 2021 United Kingdom census, the population of the City of Cambridge was 145,700; the population of the wider built-up area was 181,137. There is archaeological evidence of settlement in the area dating back to as early as the Bronze Age, and Cambridge became an important trading centre during the Roman and Viking eras. The first town charters were granted in the 12th century, although mod
England is a country that is part of the United Kingdom. It is located on the island of Great Britain, of which it covers about 62%, and more than 100 smaller adjacent islands. England shares a land border with Scotland to the north and another land border with Wales to the west, and is surrounded by the North Sea to the east, the English Channel to the south, the Celtic Sea to the south-west, and
Nearby green space: 12 parks within 1.5km — closest is Cannon's Green. via OpenStreetMap
Nearest public transit: The Broadway (bus stop, 302m). via OpenStreetMap
- Elevation 18m (59 ft)
Source: Wikipedia (state)
About this role & career path
This role aligns with O*NET Clinical Research Coordinator work (11-9121.01): protocol execution, subject coordination, documentation, and safety reporting. Senior scope typically adds multi-site oversight and cross-functional leadership rather than only bedside procedures.
Traits that fit this role
- Adaptability
- Perseverance
- Achievement Orientation
- Cooperation
- Intellectual Curiosity
Source: O*NET Work Styles (Distinctiveness Rank).
Typical preparation needed: Job Zone 4: Considerable Preparation Needed. Most of these occupations require a four-year bachelor's degree, but some do not. — via O*NET
Industry news
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- Meet Kris Benson of Superior Business Management in Cobb County - Voyage ATL
- Variety’s Business Managers Elite of 2023 - Variety
Source: O*NET (public-domain bulk data)
Salary & compensation
Workers in Management occupations earn a national median of $86,012 — via US Census ACS / Data USA
Build the skills for this role
Build strength in protocol literacy, eligibility screening, AE documentation, and IRB-facing writing. Free learning options: Saylor Academy — Health Sciences courses (free); Coursera — audit-track healthcare courses (free to learn).
Free & low-cost learning resources
- Saylor Academy — Health Sciences courses (free)
- Coursera — audit-track healthcare courses (free to learn)
Expect scenarios on eligibility screening, AE escalation, IRB/document quality, and scheduling under protocol constraints. Prepare examples of progress reports, investigator collaboration, and how you communicate study risks to subjects or caregivers.
Strong fit if you have hands-on trial ops experience and can own documentation and safety workflows for Artbio studies in a non-remote Cambridge, Massachusetts setting. Thin company DATA means validate culture, modality, and team size directly with the hiring team.
Job details above are provided by the employer/source. The sections on this page are compiled from public data sources with AI assistance.
Accommodations: if you need a workplace accommodation to apply for or perform this job, see ADA.gov or EEOC.gov for guidance on your rights and how to request one.
Listing facts
- Role Senior Clinical Trial Manager
- Employer Artbio
- Location Cambridge, Massachusetts
- Type Full Time
- Pay (from listing) Pay not listed
- Posted July 24, 2026
- Apply by August 24, 2026
- Overview Full job description on this page (265 words)
Facts above come from this job record on Get A Job.AI — not copied from third-party review sites.
Typical work in Clinical Trial Manager
Independent occupational context from O*NET (U.S. public-domain labor data). This is about the occupation, not a rewrite of this employer's posting.
- Schedule subjects for appointments, procedures, or inpatient stays as required by study protocols.
- Perform specific protocol procedures such as interviewing subjects, taking vital signs, and performing electrocardiograms.
- Assess eligibility of potential subjects through methods such as screening interviews, reviews of medical records, or discussions with physicians and nurses.
- Prepare study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.
- Inform patients or caregivers about study aspects and outcomes to be expected.
- Record adverse event and side effect data and confer with investigators regarding the reporting of events to oversight agencies.
Employer website
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1 other opening(s) at Artbio on Get A Job.AI
Occupation family: Clinical Trial Manager
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