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Consultant Clinical Scientist Jobs (NOW HIRING)

SoTalent

Clinical Scientist

Boston, MA · On-site

Clinical Scientist - Oncology Our client, a leading global pharmaceutical organization, is seeking ... consulting environment. Strong understanding of GCP and ICH guidelines alongside regional and ...

New

Integrated Resources INC

Clinical Scientist

Edison, NJ · On-site

Initiates, directs and executes all pre-clinical scientific research and/or development strategies ... Interfaces with various departments and serves as internal consultant. Additional Information All ...

Parexel

Clinical Scientist - FSP

From clinical trials to regulatory, consulting, and market access, every clinical development ... The Clinical Scientist (CS) assists the CS Protocol Lead and study team with the clinical ...

New

Icon plc

Senior Clinical Scientist

Raleigh, NC · On-site

Senior Clinical Scientist (Hematology-Oncology) ICON is a global healthcare intelligence and ... Develop and maintain collaborative working relationships with appropriate consultants and external ...

Icon plc

Senior Clinical Scientist

Dallas, TX · On-site

Senior Clinical Scientist (Hematology-Oncology) ICON is a global healthcare intelligence and ... Develop and maintain collaborative working relationships with appropriate consultants and external ...

Icon plc

Senior Clinical Scientist

Philadelphia, PA · On-site

Senior Clinical Scientist (Hematology-Oncology) ICON is a global healthcare intelligence and ... Develop and maintain collaborative working relationships with appropriate consultants and external ...

ICON

Senior Clinical Scientist

Raleigh, NC · On-site +1

Senior Clinical Scientist (Hematology-Oncology) ICON is a global healthcare intelligence and ... Develop and maintain collaborative working relationships with appropriate consultants and external ...

Syneoshealth

Clinical Scientist - Oncology

Clinical Scientist - Oncology Syneos Health is a leading fully integrated biopharmaceutical ... Engages with outside experts/consultants/advisors to coordinate the acquisition of necessary ...

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How much do consultant clinical scientist jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for consultant clinical scientist in the United States is $54.75, according to ZipRecruiter salary data. Most workers in this role earn between $40.14 and $68.27 per hour, depending on experience, location, and employer.

What is a consultant clinical scientist?

Consultant Clinical Scientists are highly qualified healthcare professionals who use their expert scientific knowledge and skills to lead clinical services, develop new diagnostic techniques, and contribute to patient care. They often specialize in areas such as genetics, pathology, or medical physics and work closely with doctors and other healthcare staff. In addition to performing advanced clinical work, they lead teams, manage services, and may be involved in research, training, and policy development. Their role is crucial in ensuring high standards of scientific practice within healthcare settings.

What are the key skills and qualifications needed to thrive as a consultant clinical scientist?

To thrive as a Consultant Clinical Scientist, you need advanced scientific knowledge, specialized clinical training (often at doctoral level), and registration with the Health and Care Professions Council (HCPC). Familiarity with laboratory information management systems (LIMS), advanced analytical techniques, and compliance with quality and regulatory standards is crucial. Leadership, effective communication, and problem-solving are vital soft skills for guiding teams and collaborating with healthcare professionals. These competencies ensure accurate diagnostics, innovation, and high standards of patient care within clinical science settings.

How do consultant clinical scientists typically collaborate with multidisciplinary teams in healthcare settings?

Consultant Clinical Scientists regularly work alongside doctors, nurses, laboratory staff, and other healthcare professionals to interpret complex scientific data and contribute to patient care decisions. They often participate in multidisciplinary meetings, provide expert advice on diagnostic testing and treatment strategies, and may lead the implementation of new technologies or protocols. Effective communication and the ability to translate scientific findings into practical clinical recommendations are essential for success in this collaborative environment.

What is the difference between Consultant Clinical Scientist vs Clinical Scientist?

AspectConsultant Clinical ScientistClinical Scientist
QualificationsTypically requires postgraduate degrees and professional registration (e.g., HCPC)Usually requires a relevant degree and postgraduate training
Work EnvironmentLeads teams in hospitals or labs, often in senior rolesPerforms testing, analysis, and research in clinical labs or hospitals
Employer & IndustryPublic health services, hospitals, research institutionsHospitals, diagnostic labs, research organizations

The main difference between a Consultant Clinical Scientist and a Clinical Scientist lies in their seniority, responsibilities, and leadership roles. Consultants typically have advanced qualifications, oversee teams, and contribute to strategic decisions, whereas Clinical Scientists focus on testing, analysis, and research within their scope. Both roles are vital in healthcare diagnostics and share similar educational backgrounds, but the Consultant role involves more leadership and specialized expertise.

How long does it take to become a consultant clinical scientist?

Becoming a consultant clinical scientist typically requires at least six to eight years of education and training, including a relevant undergraduate degree, postgraduate qualification, and extensive clinical experience. After completing a master's or doctoral degree in a related field, professionals usually undertake supervised practice and gain accreditation before progressing to a consultant role, which involves demonstrating advanced skills and leadership in the clinical environment.

What does a consultant clinical scientist do?

A consultant clinical scientist is a senior professional who applies scientific knowledge to develop, evaluate, and improve medical tests, devices, and procedures used in patient care. They often work in laboratories or hospitals, providing expert advice, overseeing clinical investigations, and ensuring compliance with regulations. The role typically requires specialized training, relevant certifications, and strong analytical and communication skills.
More about Consultant Clinical Scientist jobs

What job categories do people searching Consultant Clinical Scientist jobs look for?

The top searched job categories for Consultant Clinical Scientist jobs are:

Consultant Clinical Scientist jobs near you
Infographic showing various Consultant Clinical Scientist job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $113,877 per year, or $54.7 per hour.

Clinical Scientist

SoTalent

Boston, MA • On-site

Other

Posted 3 days ago

New

Job description

Clinical Scientist - Oncology


Our client, a leading global pharmaceutical organization, is seeking a talented Clinical Scientist to join their oncology research and development division. This role is based in Cambridge and operates under a hybrid work model.


The successful candidate will provide scientific leadership for oncology pipeline programs across major global regions. You will be instrumental in designing and executing clinical development plans that guide novel compounds through the regulatory approval process. As a key member of a cross-functional matrix team, you will ensure that scientific integrity and data findings are at the forefront of every decision.


Key Responsibilities


Serve as a scientific lead for development teams in the US and Europe, ensuring regional activities align with global strategies.


Author and contribute to critical documents including clinical protocols, study synopses, and comprehensive development plans.


Monitor and interpret data from ongoing clinical trials to provide go or no-go recommendations that impact project timelines and product labeling.


Present and defend study designs before scientific and corporate review committees.


Manage the assessment of protocol conduct and patient safety in collaboration with medical monitors and pharmacovigilance teams.


Act as a primary liaison with key opinion leaders and regulatory agencies to influence compound strategy and research programs.


Contribute to internal task forces and provide market insights based on therapeutic area expertise.


Educational and Professional Requirements


Bachelor degree with 6 years of experience, Master degree with 4 years, PharmD with 2 years, or a PhD with 1 year of experience.


Background must include clinical research or development within a pharmaceutical, CRO, academic, or healthcare consulting environment.


Strong understanding of GCP and ICH guidelines alongside regional and global regulatory requirements.


Deep knowledge of oncology or therapeutic areas relevant to specific mechanisms of action.


Proven ability to drive decision-making within multi-disciplinary and multi-regional teams.


Excellent communication and negotiation skills with the ability to simplify complex scientific information.


Proactive problem-solving skills and the ability to anticipate program challenges.


Compensation and Benefits


The anticipated base salary range for this position in Boston is 116,000 to 182,270 USD. Actual compensation will be determined based on the candidates qualifications, specialized skills, and professional experience. Our client offers a comprehensive benefits package designed to support the well-being and career growth of their employees.


Our client is an equal opportunity employer dedicated to fostering an inclusive and diverse workplace culture.

Apply