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Clinical Data Manager

Remote: 
Full Remote
Contract: 
Full time
Experience: 
Mid-level (2-5 years)
Work from: 
United States

Offer summary

Qualifications:

Bachelor’s in scientific or medical field, 2-5 years clinical data management experience, Experience in pharmaceutical or CRO industry, Hands-on clinical trials experience, Effective problem-solving and data analysis skills.

Key responsabilities:

  • Develop eCRFs and completion guidelines
  • Track study metrics and reports
  • Manage data entry and integration
  • Conduct UAT for EDC systems
  • Assist in site/user training on EDC
MMS logo
MMS SME https://www.mmsholdings.com
501 - 1000 Employees
About MMS
MMS is an award-winning, global clinical research organization (CRO) that supports leading pharmaceutical and biotech companies as well as many smaller enterprises across our spectrum of services. Having completed more than 50 submissions for drug approval over the last 5 years, we remain a top choice for sponsors who are looking for innovation and demand high quality from their CRO partners.Senior leadership at MMS has more than two decades of hands-on drug development experience which helps support program-level strategy and execution of projects across multiple therapeutic areas. Continual staff training, innovative recruitment and motivating career opportunities help MMS retain the best talent and develop a strong, client-focused workforce across all global locations.Our mission is to deliver high-quality services, rooted in good science and decades of regulatory experience, that will assist our clients in developing and marketing life-changing therapies, thereby positively affecting patients'​ lives worldwide.
See more MMS offers

Job description

Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research. 

Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit www.mmsholdings.com or follow MMS on LinkedIn.

Job Responsibilities

• Contribute to developing  eCRFs, CRF Completion Guidelines, Edit check specs, and DMP.

• Contribute to study tracking and metric reports for use by the study team• Contribute to CRF tracking and data entry, integration of external electronic data, data validation and review, query processing and resolution, adverse event and medication coding, SAE reconciliation, database lock and database QC audits.

•Contribute to user acceptance testing (UAT) of EDC and integrated systems including executing of test plan and scripts.

•Assist with preparation for training sites/users training on EDC applications, and UAT.

•End user knowledge for study conduct activities including queries management, standard reporting and extracting data.

• Learning to develop data entry screens, dynamics, edit checks and other EDC components.

Requirements

•Bachelor’s Degree in a scientific, medical, or clinical discipline or related field is required; Master’s or PhD preferred

• 2-5 years of previous experience in clinical data management

• Hands-on experience with clinical trials and pharmaceutical development preferred

•  Effective problem-solving and data analysis skills

• Experience in the pharmaceutical or CRO industry must

• Experience with query and discrepancy management required

• Has a strong attention to detail

Required profile

Experience

Level of experience: Mid-level (2-5 years)
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Hard Skills

Data ValidationPharmaceutical EngineeringUser Acceptance Testing (UAT)Query PlanningData Quality AssessmentScientific StudiesClinical TrialsClinical MedicineClinical Data ManagementData Analysis

Other Skills

  • Problem Solving
  • Detail Oriented
Are you interested?

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