Contract Senior Clinical Data Coordinator, CDM 2053098
Location: Cambridge MA (Hybrid)
Therapeutic Area: Rare Disease
Job Overview: The Sr Data Coordinator/Clinical Data Manager requires strong multitasking skills and clinical data management expertise in biotech, CRO, or pharma, with an aptitude for quickly resolving issues through collaboration.
Primary Job Responsibilities:

• Oversee clinical data integrity and timeliness, and collaborate with CROs and vendors on database development and trial data review.

• Conduct User Acceptance Testing for databases, contribute to department standards, and manage data deliverables for clinical trials.

• Coordinate data milestones, improve DM processes, and assist in cross-functional data reviews.

Primary Job Requirements:

• Requires 2-3 years of Clinical Data Management (CDM) experience, with proficiency in various EDC systems like RAVE/Veeva and knowledge of GCP and other relevant regulations.

• Experience with electronic Clinical Outcome Assessments (eCOA) and electronic Patient Reported Outcomes (ePRO) processes

• Familiarity with Interactive Response Technology (IRT) integration

About Stratacuity:
Whether you are seeking a career change or simply interested in becoming part of our network, you will appreciate the ethics guiding each Stratacuity team member. We build lasting relationships with exceptional biopharmaceutical talent and take great care to protect your personal information. Upon receiving your inquiry, you may be directly contacted by a Stratacuity team member to discuss your career goals. We will not share your information with anyone without your direct prior consent.
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