Clinical Scientist

Vita Global Sciences, a Kelly Company, is seeking a Clinical Scientist for a long-term remote engagement supporting a global pharmaceutical client. The role assists clinical study teams with scientific conduct, data review and reconciliation, protocol deviation management, meeting materials, and stakeholder collaboration across one or more studies.

Responsibilities

Assists the CS Protocol Lead and study team with the clinical/scientific conduct of clinical studies e.g, adjudication support, medical monitoring, imaging data reconciliation preparation of meeting materials, protocol deviation management

May support a single study or multiple studies

May lead a study with limited scope (e.g., Survival Follow-up)

May interact with internal and external stakeholders (study sites, committees, etc.) in support of clinical study objectives

Preferred

TA-specific experience in IDV and GSM preferred

Indication specific experience preferred

Proficient in reviewing patient data and resolving discrepancies in the following areas: adverse events, trends of adverse events, end point management, labs experience, preferred

One Note experience preferred

TA-specific experience

IDV experience

GSM experience

Indication specific experience

Patient data review

Discrepancy resolution

Adverse events management

Trends analysis

End point management

Labs experience

One Note experience

Benefits

Long-term remote engagement

Full benefit options

Eligible employees may receive medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability

401K retirement savings plan with no match

Paid time off, including holiday, vacation, and sick/personal time

Service bonus and holiday pay plans, including up to eight paid holidays per benefit year

Transit spending account

Paid sick leave under the applicable state or local plan

Company

Life sciences clinical data analytics and outsourcing services

Waltham, Massachusetts, USA

https://www.vitaglobalsciences.com/

Founded in 2014

51-200 employees

Qualifications

At least 2 years Pharmaceutical and/or clinical drug development experience (such as pharmaceutical/biopharma companies, hospital settings, research sites, clinical trial units, CRO, SMO) in the last 5 years, required

TA-specific experience required for postings in Oncology

Experience reviewing and resolving study related data issues such as: issued queries, resolved queries, accurate review of medical records, identify any errors in data by performing data review that require further clarification with the study sites, etc., required

Demonstrated oral and written communication skills

Proficiency in Microsoft Office (Outlook, Word, Excel and PowerPoint) required

Degree in Life Sciences

BS/BA/MS/PhD

Applicants must be currently authorized to work in the US on a full-time basis now and in the future

TA-specific experience in IDV and GSM preferred

Indication specific experience preferred

Proficient in reviewing patient data and resolving discrepancies in the following areas: adverse events, trends of adverse events, end point management, labs experience, preferred

One Note experience preferred

Required skills

Clinical Drug Development, Clinical Studies, Study Data Review and Issue Resolution, Medical Record Review, Adverse Event Review, Endpoint Management, Laboratory Data Review, Microsoft Office, OneNote

Preferred skills

TA-specific experience in IDV and GSM preferred, Indication specific experience preferred, One Note experience preferred

Experience

2+ years