GQR
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Position
Senior Manager, Clinical Data Management - Contractor Experience Required
8-10 years of Clinical Data Management Pay Rate
$80-$90/hr (annual equivalent: $166,000 - $187,000) Our client, an innovative clinical-stage biopharmaceutical company, is looking for a highly experienced
Clinical Data Management Contractor
to oversee data management activities for multiple clinical trials. Hybrid role for a contractor with 8-10 years of industry experience and proficiency in data management systems such as Medidata EDC. Responsibilities
Manage clinical data review processes and ensure database quality across studies. Reconcile and validate clinical databases with external datasets. Collaborate with cross-functional teams and external vendors to ensure data quality and regulatory compliance. Qualifications
Bachelor's degree in Life Sciences or a related field. Strong clinical data management expertise in a pharmaceutical or biotech setting (NO CRO Only). Extensive experience with EDC systems (Medidata preferred), CDISC, and coding standards like MedDRA and WHODRUG. This contract position offers competitive pay and the potential for a permanent role after one year. If you have a passion for improving clinical data quality and experience managing complex clinical trials, apply today! Employment type
Contract
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Senior Manager, Clinical Data Management - Contractor Experience Required
8-10 years of Clinical Data Management Pay Rate
$80-$90/hr (annual equivalent: $166,000 - $187,000) Our client, an innovative clinical-stage biopharmaceutical company, is looking for a highly experienced
Clinical Data Management Contractor
to oversee data management activities for multiple clinical trials. Hybrid role for a contractor with 8-10 years of industry experience and proficiency in data management systems such as Medidata EDC. Responsibilities
Manage clinical data review processes and ensure database quality across studies. Reconcile and validate clinical databases with external datasets. Collaborate with cross-functional teams and external vendors to ensure data quality and regulatory compliance. Qualifications
Bachelor's degree in Life Sciences or a related field. Strong clinical data management expertise in a pharmaceutical or biotech setting (NO CRO Only). Extensive experience with EDC systems (Medidata preferred), CDISC, and coding standards like MedDRA and WHODRUG. This contract position offers competitive pay and the potential for a permanent role after one year. If you have a passion for improving clinical data quality and experience managing complex clinical trials, apply today! Employment type
Contract
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