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Weekend Clinical Trial Rn Jobs in Worcester, MA (NOW HIRING)

Director, Clinical Scientist

Needham, MA ยท On-site

$200K - $260K/yr

Leads the clinical/scientific design and execution of assigned clinical trial(s), partnering ... Advanced degree in life sciences or clinical practice experience highly preferred (e.g., R.N., PhD ...

Leads the clinical/scientific design and execution of assigned clinical trial(s), partnering ... Advanced degree in life sciences or clinical practice experience highly preferred (e.g., R.N., PhD ...

Senior Director, Clinical Scientist

Needham, MA ยท On-site

$260K - $300K/yr

Leads the clinical/scientific design and execution of assigned clinical trial(s), partnering ... Advanced degree in life sciences or clinical practice experience highly preferred (e.g., R.N., PhD ...

Senior Director, Clinical Scientist

Needham, MA ยท On-site

$260K - $300K/yr

Leads the clinical/scientific design and execution of assigned clinical trial(s), partnering ... Advanced degree in life sciences or clinical practice experience highly preferred (e.g., R.N., PhD ...

RN Weekend Baylor

Newton, MA ยท On-site

$45/hr

On-Call Home Health Registered Nurse (RN) Job Type: Full-Time 24 hours - Saturday, Sunday Location ... Home Health Clinical Manager Salary Range: Starting at $45/hr - Salary position! Home is Where the ...

Travel Nurse RN - Telemetry

Palmer, MA ยท On-site

$2.0K - $2.8K/wk

TNAA TotalMed RN is seeking a travel nurse RN Telemetry for a travel nursing job in Palmer ... clinicians of all specialties in all 50 states. They offer local and travel jobs and match ...

Travel Nurse RN - Telemetry

Palmer, MA ยท On-site

$2.0K - $2.8K/wk

TNAA TotalMed RN is seeking a travel nurse RN Telemetry for a travel nursing job in Palmer ... clinicians of all specialties in all 50 states. They offer local and travel jobs and match ...

Travel Behavioral Health RN

Worcester, MA ยท On-site

$1.7K - $2.4K/wk

TNAA TotalMed RN is seeking a travel nurse RN Psychiatric for a travel nursing job in Worcester ... The Psychiatric Nurse also collaborates with clinical and case management staff to coordinate care ...

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Weekend Clinical Trial Rn information

See Worcester, MA salary details

$28

$62

$95

How much do weekend clinical trial rn jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for weekend clinical trial rn in Worcester, MA is $62.38, according to ZipRecruiter salary data. Most workers in this role earn between $50.62 and $70.29 per hour, depending on experience, location, and employer.

What is a Weekend Clinical Trial RN?

Weekend Clinical Trial RNs are registered nurses who work primarily on weekends to support clinical research studies. Their responsibilities include administering investigational treatments, monitoring patient safety, collecting data, and ensuring protocol compliance. They collaborate with research teams, patients, and other healthcare providers to facilitate trials and maintain high standards of care. This role is crucial for studies that require continuous patient oversight and data collection outside of standard weekday hours.

What are some unique challenges of working as a Weekend Clinical Trial RN, and how can I prepare for them?

As a Weekend Clinical Trial RN, you may encounter challenges such as limited onsite support, managing urgent protocol issues, and balancing patient care with strict research timelines. Since weekends often have fewer staff members present, strong communication and problem-solving skills are essential. To prepare, familiarize yourself with study protocols in advance, establish clear lines of communication with the principal investigator and other team members, and ensure you are comfortable with electronic data capture systems. Being proactive and organized will help you provide excellent patient care while maintaining compliance with research requirements.

What are the key skills and qualifications needed to thrive as a Weekend Clinical Trial RN, and why are they important?

To thrive as a Weekend Clinical Trial RN, you need a current RN license, clinical nursing experience, and a solid understanding of Good Clinical Practice (GCP) guidelines. Familiarity with clinical trial management systems, electronic data capture (EDC) tools, and protocol documentation is typically required. Strong attention to detail, organizational skills, and effective communication are vital soft skills for coordinating with research teams and ensuring regulatory compliance. These skills and qualities are crucial for maintaining patient safety, data integrity, and adherence to study protocols during weekend trial operations.

What is the difference between Weekend Clinical Trial Rn vs Weekend Research Nurse?

AspectWeekend Clinical Trial RnWeekend Research Nurse
CredentialsRegistered Nurse (RN) license, clinical trial trainingRegistered Nurse (RN) license, research-specific training
Work EnvironmentClinical trial sites, hospitals, research facilitiesResearch centers, hospitals, clinical research units
Employer & IndustryPharmaceutical companies, research organizationsAcademic institutions, research organizations
Work ScheduleWeekend shifts, flexible hoursWeekend shifts, flexible hours

Both roles involve RN credentials and work in research settings, often during weekends. The main difference lies in the focus: Weekend Clinical Trial Rns primarily support clinical trial protocols, while Weekend Research Nurses may be involved in broader research activities. Both roles are essential in advancing clinical research and typically require similar certifications and work environments.

What cities near Worcester, MA are hiring for Weekend Clinical Trial Rn jobs?

Cities near Worcester, MA with the most Weekend Clinical Trial Rn job openings:

Infographic showing various Weekend Clinical Trial Rn job openings in Worcester, MA as of July 2026, with employment types broken down into 86% Full Time, and 14% Part Time. Highlights an 100% In-person job distribution, with an average salary of $129,751 per year, or $62.4 per hour.

Director, Clinical Scientist

Needham, MA โ€ข On-site

Verastem
51 - 200 employees

$200K - $260K/yr

Full-time

Posted 9 days ago


Job description

The Director, Clinical Scientist provides clinical and scientific leadership for assigned oncology studies and programs. This individual serves as a key member of Study and Program Teams, leading clinical/scientific execution, data review and interpretation, and development of study and regulatory documents to support development strategy and potential market authorization applications.
Responsibilities
  • Leads the clinical/scientific design and execution of assigned clinical trial(s), partnering closely with cross-functional study and program teams.
  • Ensures clinical data integrity through hands-on, ongoing review, analysis, and interpretation of safety, efficacy, pharmacokinetic, biomarker, and other study data; identifies emerging trends and translates study-level findings into program-level insights and recommendations.
  • Oversees clinical science support from partner CROs and creates and refines data review and cleaning processes, tools, and workflows to improve efficiency, consistency, and data quality.
  • Authors and leads key study and clinical/regulatory documents, including protocols and synopses, informed consent forms, investigator brochures, briefing books, safety updates, clinical study reports, and clinical sections of regulatory submissions and responses.
  • Contributes to integrated clinical development plans and study/program strategy, including key development options, risks, and decision points.
  • Partners with investigators and internal/external stakeholders to support protocol interpretation, appropriate scientific/medical oversight, and compliance with GCP/GxP and applicable regulatory requirements.
  • Leads or supports investigator meetings, protocol training, advisory boards, steering committees, and other scientific forums; develops and delivers clear presentations for internal and external audiences.
  • Supports scientific communication through literature review and development/review of abstracts, presentations, and manuscripts; maintains current knowledge of oncology, clinical development, and the external regulatory/scientific environment, and develops strong collaborative relationships across Verastem and with external scientific partners.

Required qualifications
  • Master's degree (MS) in life sciences or a related discipline with 12+ years of relevant work experience required.
  • Progressive biotech/pharma clinical development experience, with demonstrated leadership in oncology clinical strategy, study execution, and clinical data and safety analysis.
  • Strong knowledge of Good Clinical Practices (GCP/GxP), clinical trial design, the global drug development process, and current regulatory expectations (e.g., FDA and EMA).
  • Demonstrated ability to lead and influence cross-functional matrix teams, work independently, and exercise sound clinical/scientific judgment in a fast-paced entrepreneurial environment.
  • Excellent analytical, interpersonal, verbal communication, influencing, and presentation skills, including the ability to distill complex information into key considerations and decision points.
  • Ability to travel up to 20% of the time.

Preferred qualifications
  • Advanced degree in life sciences or clinical practice experience highly preferred (e.g., R.N., PhD, PharmD).
  • Prior experience with global clinical trials and NDA/BLA or other major regulatory submissions preferred.
  • Experience in oncology drug development across multiple stages of clinical development preferred.

The base salary range ($200,000 - $260,000) provided reflects our current estimate of what we anticipate paying for this position. Your actual base salary will be based on several factors, including job-related skills, experience, internal equity, relevant education or training, location, and market dynamics. In addition, you will be eligible for an annual bonus, equity compensation, and a competitive benefits package.