Late Stage Oncology Clinical Scientist

AECOM; New York (NY); Hybrid; USD 102,000 - 172,000; Full time

Job summary

A leading company in the field of oncology is seeking a Clinical Development Professional to oversee clinical trials and ensure data quality in their Late-Stage Oncology portfolio. The role requires a strong understanding of scientific processes and the ability to collaborate effectively with colleagues in a dynamic team environment. Successful candidates will hold relevant degrees and have experience in the clinical research space, particularly in oncology. This hybrid position necessitates a commitment to being onsite approximately 2.5 days per week.

Benefits

401(k) plan with matching contributions

Paid vacation and personal days

Health benefits including medical, dental, and vision

Comprehensive benefits and programs

Qualifications

• Relevant PhD or PharmD with 1 year experience in clinical roles.
• MS with 2 years experience, or BA/BS with 5 years experience.
• Knowledge of clinical procedures, ICH guidelines, and GCP.

Responsibilities

• Provide support for clinical trial oversight, ensuring data integrity.
• Author clinical documents and support colleagues in clinical execution.
• Analyze emerging safety profiles and adhere to SOPs and regulations.

Skills

Scientific writing

Communication skills

Data analysis

Collaborative teamwork

Education

PhD or PharmD

MS

BA/BS

Tools

JReview

RAVE

SpotFire

Job description

**Position Summary**

You will be responsible for providing support of scientific oversight, data integrity and quality of clinical trial(s) in support of the development strategy for programs within the Late-Stage Oncology portfolio.

**Key Responsibilities**

+ Clinical development professional maintaining current scientific and clinical knowledge in the specific therapeutic and disease area(s) of assignment.

+ Support other clinical and medical colleagues, clinical operations and other functional lines for the successful implementation and execution of the clinical trial(s) within the assigned program.

+ Responsible for providing support of scientific oversight, data integrity and quality of the clinical trial(s).

+ Contributes and support other clinical and medical colleagues, with authoring protocols, study level informed consent documents, site training materials, and other clinical and regulatory documents; as appropriate.

+ Reviews and queries safety and efficacy data in support of the clinical data review strategy and collection of quality data and review of emerging clinical data and trends.

+ In close partnership with medically qualified colleague/s, analyzes the emerging safety profile of the drug, keeping the clinical and safety colleagues informed of changes in the safety profile as they occur in the assigned trial(s).

+ Follows relevant SOPs and regulations, has an excellent understanding of and complies with applicable trainings, seeks opportunities to further improve quality and efficiency of clinical procedures; actively participates in portfolio- and enterprise level workgroups aimed at optimizing PFE clinical development procedures.

**Minimum Qualifications/Key Skills**

+ Relevant PhD or PharmD and a minimum of 1 year of experience in a similar role in industry/CRO, **OR**

+ MS and a minimum of 2 years of experience in a similar role in industry/CRO, **OR**

+ BA/BS and a minimum of 5 years of experience in a similar role in industry/CRO.

+ Knowledge of clinical procedures, ICH guidelines, GCP and familiarity with FDA, EMA, and global regulations.

+ Strong scientific writing skills and communication skills (written and verbal)

+ Track record of scientific productivity as evidenced by publications, posters, abstracts and/or presentations.

+ Some understanding of related disciplines, e.g., Clinical Operations, Safety, Biostatistics, Regulatory, Study Management, Pre-Clinical, Pharmacology, Quality Assurance.

+ Experience building consensus and driving change across all levels of the organization including senior management.

+ Experience working collaboratively in a fast-paced, team-based matrix environment as well as independently

+ Experience performing complex data analyses using JReview, RAVE, SpotFire, SOCs-PRO or other similar platform

**Preferred Qualifications**

+ Industry/CRO Clinical Research experience in Oncology

+ Oncology Fellowship or experience in academia

**Work Location Assignment:** Hybrid - must be onsite an average of 2.5 days/week

The annual base salary for this position ranges from $102,900.00 to $171,500.00. 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. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life's moments. Benefits offered include a 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, and 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.

Relocation assistance may be available based on business needs and/or eligibility.

**Sunshine Act**

Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.

**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.

Medical

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