CEO,Jannatul Ferdous
Who we are

We are specialized in Pharma , Biotech and IT services and are dedicated to providing the best temporary, temporary-to-hire and full-time Technology, Business Professional, Scientific and Clinical Development professional talent for large and midsize enterprise. Our recruiters have years of training and experience in understanding the exact skill sets necessary for placing IT, Scientific and Clinical development candidates in your company. We have an vast network within the industry, enabling us to target and recruit qualified candidates in a timely and efficient manner. Our job is to find top talent for different roles; we work closely with you to reach your career  goals and will leverage our network to elevate your professional goals.


The Veritas also provides payroll services, as a practical matter, payroll services are a commodity offering. As a result, we strive to provide pricing that is transparent and fair given the fact that the statutory costs are widely known.

The Veritas Healthcare Solutions LLC offers a complete recruiting solution of consultants for clinical trials and research projects. We take care to provide the most experienced and talented consultants in the field of clinical research staffing, pharmaceutical staffing and healthcare staffing.


         Pharmacovigilance is the  practice of monitoring the effects of medical drugs after they have been licensed for use, especially in order to identify and evaluate previously unreported adverse reactions.

Looking for Job

Current Job openings :

Multiple Drug Safety Associate Positions for health care professionals

Experience with data entry into drug safety databases such as ARISg/ARGUS, preferred.
Execution of local activities relevant to the management of safety data.
Maintain local documentation as required by legislation (including archiving/tracking/retrieval) – lifting of boxes; .
Support the submission and distribution of reports and relevant tracking Support distribution and tracking of distribution of Follow-Up letters; .
Support inspection preparedness activities policies and practices as per Company SOPs;
Consistently apply Archiving policies as per Company SOP.

Regulatory Affairs Associate(Multiple Positions)

A minimum of 6 months regulatory Affairs experience required; Experience associated with managing or publishing of global regulatory submissions, including FDA (eCTD) and/or EMA (National, MRP and CTAs) is required.
Establishing Dossier Plans for the assigned Global submission types as needed to support the lifecycle of one or more products.
Ensuring dispatch/distribution in compliance with due dates to Health Authorities and/or Local Operating Companies, as applicable, tracking submission events/activities in appropriate systems/tools.
Support development of departmental work practices, process enhancements, and associated training materials…

Clinical Research Associate & Specialists Positions

Responsible for all aspects of clinical study operations for assigned clinical projects according to the strategy defined by leadership of Clinical Research team. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
Coordinates clinical operations including: design, initiation, coordination of clinical trials to support regulatory submissions, as well as post-market clinical trials.
Identify and qualify study centers

Clinical SAS Programmers (Various positions)

Requires Exp. SAS supporting clinical trials MS Statistics/BS Computer Science or Math
Utilizes BI SOPs and guidelines, trial protocols, annotated case report forms, Oracle*Clinical study definitions, trial and project data handling rules and standards, and Statistical Analyses Plans in preparation for the programming of the Data Quality Review Plan (DQRP) and the safety and efficacy tables, listings and graphs (TLG) required for the Clinical Trial Report (CTR) and the associated Analyses Data Sets (ADS). Gains specific knowledge about the users’ environment, data, software and hardware needs
Create and maintain SAS programs to support CDISC SDTM data validation on clinical trial databases


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