Clinical data management is essential to the integrity and success of clinical trials. This publication invites registrations from experienced data professionals interested in contributing to regulated clinical research environments where meticulous data handling directly supports patient safety and regulatory compliance. Roles of this type coordinate data collection, validation and reporting across trial sites, working within GCP and FDA frameworks to ensure data quality at every step. Please note the content of this advert does not represent a live vacancy. About the opportunity This is an opportunity to register your interest in future Clinical Data Manager contract positions supporting clinical trial operations in the life sciences sector. Roles of this type sit within research environments where data integrity underpins regulatory submissions and patient outcomes. The work could involve managing electronic data capture (EDC) systems, coordinating with clinical sites on data queries and discrepancies, and ensuring audit trails and regulatory documentation meet FDA and ICH-GCP standards. You could work across multi-site trials, bringing structure and accountability to the data lifecycle from enrollment through database lock. Typical role overview

Location:

New York, New York, USA Type:

Contract

•

Full-time Rate:

$560-$800 per day, dependent on experience and trial complexity

Domain:

Clinical trials

• Data management

• Life sciences What you would do Typical responsibilities could include: Managing electronic data capture (EDC) systems and coordinating data collection across clinical trial sites Identifying, documenting and resolving data discrepancies through site queries and audit trail reviews Validating trial data for completeness, accuracy and compliance with protocol and regulatory requirements Supporting data lock preparation, including final reconciliation and quality control checks Maintaining detailed documentation of data management activities and audit trails for regulatory inspection Communicating data issues and resolutions to clinical operations, sponsors and regulatory teams Contributing to standard operating procedures (SOPs) and process improvements in data management workflows What you could bring Most roles of this type require the following: Must-have 2-5 years of clinical data management experience in regulated trial environments Working knowledge of Good Clinical Practice (GCP), FDA regulations and ICH guidelines Proficiency with electronic data capture (EDC) systems and clinical trial management software Strong attention to detail, organizational skills and ability to manage multiple data streams Degree in Life Sciences, Data Science or a related field, or equivalent professional certification (such as ACRP CDMP or equivalent) Authorization to work in the United States Nice-to-have Experience with SAS, SQL or other statistical analysis tools Familiarity with Common Technical Document (CTD) or eCopy submissions Experience in Phase II, Phase III or Phase IV trials Knowledge of CDISC standards (SDTM, ADaM) What roles of this type could offer Most roles of this type offer the following, dependent on the industry and seniority of the role: Contribution to clinical research that may support regulatory approval and patient access to new therapies Exposure to multi-site trial operations and regulatory workflows Potential for contract-to-permanent conversion or extended engagement, where trial scope and funding allow Professional development in compliance, data standards and clinical operations Flexibility and contract-based engagement suited to project-driven research environments About Specialist Staffing Group Specialist Staffing Group connects healthcare and life sciences professionals with contract and permanent opportunities across clinical research, regulatory affairs, quality and operations. We support clinical trials, medical device companies and pharmaceutical organizations in building specialized teams that deliver compliant, patient-centered research and development. How to register interest If you are interested in being added to our database to be considered for future opportunities, registering is quick and easy. No cover letter required. We will be in touch when we are instructed on these roles to discuss the next step in your career. Please note that the content of this advert does not represent a live vacancy or any guarantee of future vacancies, and by responding to this advert you agree to us adding your details to our database for future opportunities.