Senior Clinical Data Manager Clinical-stage Biotech Remote

Carbyne; Remote; EUR 70.000 - 90.000; Vollzeit

Zusammenfassung

An innovative biotech company is seeking a Senior Clinical Data Manager to contribute to the development of groundbreaking immuno-oncology therapies. This full-time remote position requires a Bachelor's or Master's degree in Life Sciences, 4-5 years of Clinical Data Management experience, and proficiency in English. Key responsibilities include overseeing data management tasks, ensuring data quality, and liaising with CROs. Join a passionate team to help bring novel treatment options to patients globally.

Qualifikationen

• At least 4-5 years of experience with Clinical Data Management.
• Prior experience in CRO-oversight, Biostatistics, and oncology is a plus.

Aufgaben

• Perform Clinical Data Management tasks.
• Ensure Data Validation Plan is aligned with study protocol.
• Define and perform data quality checks.
• Lead data transfer activities and oversee vendors.
• Analyze preclinical lab or clinical data.

Kenntnisse

Clinical Data Management

Data Validation

Data Quality Checks

Analytical Skills

CRO Oversight

Proficiency in English

Ausbildung

Bachelor's or Master's Degree in Life Sciences or Statistics

Jobbeschreibung

Our partner is an emerging international clinical-stage biotech company developing first-in-class immuno-oncology therapies. Their dedicated international team is looking for its newest member to join as Senior Clinical Data Manager to help bring innovative treatment options to patients worldwide. This newly created full-time remote role provides the opportunity to contribute to the development of biotech innovations never seen before.

Responsibilities

• Clinical Data Management tasks
• Ensuring Data Validation Plan is aligned with CRF study protocol and SAP etc.
• Defining and performing data quality checks
• CRF review
• Develop internal processes for data acquisition and data management
• Overlooking and leading data transfer activities e.g., data transfer agreements and QC checks
• Vendor / CRO oversight
• Supporting vendor qualification for DM
• Act as point of contact for CROs and labs for DM activities for multiple studies
• Providing oversight of data collection and management
• Helping with analyzing preclinical lab or clinical data

Qualifications

• Bachelors or Masters Degree in Life Sciences or Statistics
• At least 4-5 years of experience with Clinical Data Management
• Proficiency in written and spoken English
• Eye for detail analytical skills motivation to work at a clinical-stage biotech
• Prior experience in CRO-oversight, Biostatistics and the field of oncology can be a plus

Should you be interested in this position please let us know by submitting your CV via the advertisement - our colleagues will soon contact you with the details.