Clinical Scientist, Hepatology Clinical Development

GlaxoSmithKline

Waltham (MA)

Sur place

USD 151 000 - 252 000

Plein temps

Il y a 2 jours
Soyez parmi les premiers à postuler

Obtenez une réponse de cet employeur

Votre CV et votre lettre de motivation, adaptés exactement à ce que l’employeur recherche.

Passez les filtres ATS

Avantages offerts par ce poste

Annual bonus
Health care
Pension plan
Share savings plan

Résumé du poste

GlaxoSmithKline is seeking a Clinical Scientist in Hepatology Clinical Development. The role is on-site in either Waltham, MA, USA or London, UK, with no hybrid/remote options.

You will design, conduct, and report clinical studies and collaborate across Medical Monitoring, Regulatory Affairs, Biostatistics, Data Management, and external investigators. The position requires a PharmD/PhD/MD or equivalent and a minimum of 3 years in clinical research or drug development; strong GCP knowledge and

Qualifications

  • Minimum of a PharmD, PhD, MD, or equivalent.
  • A minimum of 3 years of clinical research or drug development experience.

Responsabilités

  • Contribute to clinical development plans and study design.
  • Support protocol, amendment, and informed consent development.
  • Evaluate emerging scientific and competitive data.
  • Participate in feasibility and site selection activities.
  • Partner with Clinical Operations to oversee study conduct.
  • Monitor enrollment, protocol deviations, and study performance.
  • Prepare and review CSRs, abstracts, and presentations.

Connaissances

Agile Thinking
Clinical Development
Clinical Trial Designs
Leadership
Project Management
Teamwork
Risk Management
Time Management

Formation

PharmD/PhD/MD or equivalent

Description du poste

We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programs, pension plan membership, and shares and savings programme. We embrace modern work practices; our Performance with Choice programme offers a remote or hybrid working model, empowering you to find the optimal balance between remote and in-office work.

Discover more about our company-wide benefits and life at GSK on our webpage Life at GSK | GSK

Find out more about GSK and R&D: Our approach to R&D

Clinical Scientist, Hepatology Clinical Development

The Clinical Scientist is a key member of the Clinical Development team and contributes to the design, execution, analysis, and reporting of clinical studies across all phases of development. Working closely with Clinical Development, Medical Monitoring, Clinical Operations, Biostatistics, Data Management, Regulatory Affairs, and external investigators, the Clinical Scientist provides scientific and operational expertise to ensure successful study execution and generation of high‑quality clinical data.

This role can be in either Waltham, MA in the US or GSK Headquarters in London, UK and requires working on‑site. Hybrid or remote work options are not available for this position.

This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
  • Contribute to clinical development plans and study design.
  • Support protocol, amendment, and informed consent development.
  • Evaluate emerging scientific and competitive data.
  • Participate in feasibility and site selection activities.
  • Partner with Clinical Operations to oversee study conduct.
  • Monitor enrollment, protocol deviations, and study performance.
  • Participate in investigator meetings and site engagement activities.
  • Support issue identification and resolution.
  • Review safety, efficacy, biomarker, and PK/PD data.
  • Identify trends and data quality concerns.
  • Collaborate on database lock and analysis activities.
  • Support interpretation of study results.
  • Prepare and review CSRs, abstracts, and presentations.
  • Support advisory boards and scientific congress activities.
  • Contribute to Investigator's Brochures and regulatory submissions.
Basic Qualifications

We are looking for professionals with these required skills to achieve our goals:

  • Minimum of a PharmD, PhD, MD, or equivalent.
  • A minimum of 3 years of clinical research or drug development experience.
Preferred Qualifications

Please note the following skills are not necessary, just preferred, if you do not have them, please still apply:

  • Experience drafting or reviewing clinical study protocols, informed consent forms, and clinical study reports.
  • Experience providing medical monitoring or clinical safety oversight.
  • Demonstrated ability to work effectively in cross-functional teams and with external partners.
  • Strong understanding of GCP and global regulations.
  • Excellent communication and collaboration skills.
Skills

Agile Thinking, Clinical Development, Clinical Trial Designs, Decision Making, Fostering Collaboration, Influencing Without Authority, Leadership, Matrix Leadership, Mentorship, People Management, Project Management, Risk Management, Strategic Thinking, Teamwork, Time Management* If you are based in Cambridge, MA; Waltham, MA; Rockville, MD; or San Francisco, CA, the annual base salary for new hires in this position ranges $150,975 to $251,625. The US salary ranges take into account a number of factors including work location within the US market, the candidate's skills, experience, education level and the market rate for the role. In addition, this position offers an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. Available benefits include health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and paid caregiver/parental and medical leave. If salary ranges are not displayed in the job posting for a specific country, the relevant compensation will be discussed during the recruitment process.

Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases - to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we're committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

If you require an accommodation or other assistance to apply for a job at GSK, please contact the appropriate Recruitment Staff by emailing us at usrecruitment.adjustments@gsk.com

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.

Important notice to Employment businesses/ Agencies

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

Obtenez votre examen gratuit et confidentiel de votre CV.

ou faites glisser et déposez votre fichier ici.

Similar jobs

Postes similaires à comparer

Clinical Scientist, Hepatology Clinical Development
Clinical Scientist, Hepatology Clinical Development

1925 GlaxoSmithKline LLC • Waltham (MA)

Sur place
USD 151 000 - 252 000
Healthcare
Pension plan
Shares & Savings program
Medical Director, Clinical Development, Hepatology
Medical Director, Clinical Development, Hepatology

Women In Bio • Central (PA)

Hybride
USD 223 000 - 371 000
Clinical Development Medical Director- Hepatology
Clinical Development Medical Director- Hepatology

GSK • Boston (MA)

Hybride
USD 203 000 - 338 000
Medical Director Clinical Development- Respiratory
Medical Director Clinical Development- Respiratory

Regulatory Toolkit • Waltham (MA)

Hybride
USD 241 000 - 375 000
Annual bonus
Share-based long term incentive
Health care and other insurance
+4
Clinical Development Medical Director- Hepatology
Clinical Development Medical Director- Hepatology

Regulatory Toolkit • Boston (MA)

Hybride
USD 223 000 - 371 000
Medical Director Clinical Development- Aging
Medical Director Clinical Development- Aging

GlaxoSmithKline • Waltham (MA)

Hybride
USD 190 000 - 316 000
Clinical Development Medical Director- Hepatology
Clinical Development Medical Director- Hepatology

GlaxoSmithKline • Upper Providence

Hybride
USD 202 500 - 371 250
Medical Director, Oncology Clinical Development - Lung & Head/Neck Cancers
Medical Director, Oncology Clinical Development - Lung & Head/Neck Cancers

GlaxoSmithKline • Waltham (MA)

Sur place
USD 223 000 - 371 000
Medical Director, Clinical Development, Hepatology
Medical Director, Clinical Development, Hepatology

GlaxoSmithKline • Philadelphia

Hybride
USD 223 000 - 371 000
Health care
Retirement benefits
Paid holidays
+2
Medical Director, Oncology Clinical Development - Lung & Head/Neck Cancers
Medical Director, Oncology Clinical Development - Lung & Head/Neck Cancers

Regulatory Toolkit • Lower Providence Township (PA)

Sur place
USD 223 000 - 371 000