Clinical Development Scientist, Manager-Inflammation and Immunology (I&I)

Pfizer; Cambridge (MA); Híbrido; USD 106.000 - 177.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

401(k) plan with Pfizer Matching

Paid vacation

Holiday and personal days

Paid caregiver/parental and medical-le

Health benefits (medical, dental, etc)

Descripción de la vacante

Pfizer is seeking a Clinical Development Scientist to support the development and execution of small and novel studies in the I&I area. You will contribute on clinical study teams, collaborating with operations, medical monitors, biostatistics, and digital medicine to ensure enrollment and timely study delivery.

Ideal candidates hold a PharmD/PhD or advanced degree with 2+ years of industry experience, and demonstrate strong knowledge of GCP/ICH, plus excellent communication skills.

Formación

• PharmD/PhD or MS/MA/MSN with industry experience in clinical studies.
• Comprehensive knowledge of GCP and ICH guidelines.
• Strong communication and interpersonal skills in a pharma setting.

Responsabilidades

• Support development and execution of simple to minimally complex clinical studies; assist senior scientists on complex components.
• Prepare and review study documents (protocols, consent forms, training materials).
• Support clinician data review activities; assist with safety data collection for reviews.
• Provide technical support for clinical issues with internal/external collaborators (in collaboration with the Global Development Lead).
• Maintain open, transparent communication within the study team to support timely study completion.

Conocimientos

GCP/ICH knowledge

Strong communication

Pharma/biopharma environment knowledge

Clinical study support

Educación

PharmD/PhD in a related discipline

MS/MA/MSN with 2+ years of experience in industry

BS/BA/BSN with 4+ years of experience in industry

Herramientas

Microsoft Word

Microsoft PowerPoint

Microsoft Excel

Descripción del empleo

POSITION SUMMARY

You will support the development and execution of one or more less complex studies for small molecule and/or novel biological therapies in the I&I therapeutic area. You may participate as an individual contributor (often in partnership with and/or under the mentorship of a more senior Clinical Development Scientist) on clinical study teams to support enrollment and study delivery timelines. You will work with other functional disciplines as needed (e.g., Clinical Operations, Global Clinical Leads/Medical Monitors, Biostatistics/Data Management, Clinical Pharmacology, and Digital Medicine). You may be a member of clinical sub-teams to ensure collaboration and seamless connectivity across functions.

POSITION RESPONSIBILITIES

• Support the development and execution of simple to minimally complex clinical studies; on more complex studies, support a more senior Clinical Development Scientist by taking responsibility for assigned components of the overall clinical team's deliverables.
• Support the preparation and review of study-related documents, including but not limited to clinical protocols, informed consent documents, and study training materials.
• Support clinician data review activities; on more complex studies, work with a more senior Clinical Development Scientist to collect and collate safety data for safety review meetings and ongoing monthly data reviews in accordance with the data review plan.
• Provide technical support for clinical issues raised by internal and external collaborators, investigators, consultants, and contractors in collaboration with the Global Development Lead (GDL), as needed.
• Collaborate with the study team to maintain open and transparent communication and support successful study completion.

MINIMUM QUALIFICATIONS

• PharmD/PhD in a related discipline OR MS/MA/MSN and 2+ years of related industry clinical study experience OR BS/BA/BSN and 4+ years of related industry clinical study experience
• Comprehensive knowledge of GCP and ICH guidelines.
• Good understanding of the pharmaceutical/biopharmaceutical environment and drug development.
• Strong communication and interpersonal skills.
• Proficiency in Microsoft Office applications, including Word, PowerPoint, and Excel.

PREFERRED QUALIFICATIONS

• Experience in a clinician-type role or clinical operations-type role including experience executing clinical studies
• Project Management experience
• Relocation support available

Work Location Assignment

Hybrid-- Will work on-site an average of 2.5 days per week and must live within commuting distance to the site.

Salary and Bonus

The annual base salary for this position ranges from $106,000.00 to $176,600.00. In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 15.0% of the base salary and eligibility to participate in our share based long term incentive program.

Benefits

We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life's moments.

• 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution
• paid vacation
• holiday and personal days
• paid caregiver/parental and medical leave
• health benefits to include medical, prescription drug, dental and vision coverage

Learn more at Pfizer Candidate Site - U.S. Benefits | (uscandidates.mypfizerbenefits.com).

Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States. This role is posted in multiple locations. If you are applying for the role in an secondary job posting location where pay transparency regulations apply, your Talent Advisor will share the local pay information with you during the first interview. Relocation assistance may be available based on business needs and/or eligibility. Candidates must be authorized to be employed in the U.S. by any employer.

EEO & Employment Eligibility

Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.

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Medical Pfizer careers are like no other. In our culture of individual ownership, we believe in our ability to improve future healthcare, and potential to transform millions of lives. We're looking for new talent to join our global community, to unearth new innovative therapies that make the world a healthier place.