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Clinical Scientist/Clinical Research Consultant at ClinChoice

, , Mexico -

Full Time

Start Date

Immediate

Expiry Date

29 Dec, 25

Salary

0.0

Posted On

30 Sep, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research, Medical Monitoring, Data Reconciliation, Protocol Deviation Management, Communication Skills, Microsoft Office, Data Review, Adverse Events Management, Imaging Data, Study Management, Stakeholder Interaction, Pharmaceutical Experience, Oncology Experience, Indication Specific Experience, Query Resolution, Trends Analysis

Industry

Pharmaceutical Manufacturing

Description

Clinical Scientist (Clinical Research/Clin Ops) Description of Services 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 Minimum Years of Experience At least 2 year 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 IDV and GSM preferred. Indication specific experience preferred 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 Proficient in reviewing patient data and resolving discrepancies in the following areas such as adverse events, trends of adverse events, end point management, labs experience preferred Demonstrated oral and written communication skills Proficiency in Microsoft Office (Outlook, Word, Excel and PowerPoint) required. One Note experience preferred. Educational Requirements Degree in Life Sciences BS/BA/MS/PhD

Responsibilities

Assist the CS Protocol Lead and study team with the clinical/scientific conduct of clinical studies. May support a single study or multiple studies and interact with internal and external stakeholders in support of clinical study objectives.