Inventiv Health jobs

Qualifications: Significant experience in clinical trial oversight and authoring clinical development documents/summarizing clinical study results. Must have understanding of... more

administrative duties for the Employee Health team. Treat illness/ injuries. Manage ... and evaluates programs to meet employee health wellness initiatives. Provides direct... more

Clinical Data Manager II (6m)-Responsible for providing timely and professional ongoing quality management of clinical trial data by identifying errors/inconsistencies in CRF data... more

Title: Medical Safety Monitor in Santa Ana, CA. Primary Job Function: The Medical Safety Monitor is responsible for the oversight of the adverse events and product experiences... more

Submissions Module (ESM) from European Health Authorities on behalf of Country Offices that are not online with Argus and other submitters as necessary. Monitor electronic... more

Job Title: Safety Operation Physician in South San Francisco, CA. Duties: Accountable for the medical review, code check and assessment (including listedness and labeling) and... more

? Develops relationships with key opinion leaders and applies their input to enhance study design and protocols. ? Serves as a medical/scientific consultant to marketing, research... more

Description Provides support for the review of potential adverse events of company products. Reviews and assesses domestic/international clinical trials and post-marketing... more

Associate Director of Marketing Philadelphia Area The position will have primary responsibility for the development and execution of the consumer strategy supporting the launch of... more

and electronic submissions. Help respond to health authority inquiries for submitted dossiers. Establish and maintain sound working relationship and effective communications... more

and electronic submissions. Help respond to health authority inquiries for submitted dossiers. Establish and maintain sound working relationship and effective communications... more

Responsible for managing global Supply Chain activities in support of national and international phase I IV clinical trials, including Investigator Initiated Studies (IIS). more

Title- Sr. Leader, Digital /Web Strategy location- Dayton, OH (relo provided) Consultant- Eda Zullo, ezullo@smithhanley.com My client, a well known corporate financial services... more

Job Title: Drug Safety Scientist in South San Francisco, California. Department: Drug Safety - Development Reporting to: Sr. Drug Safety Scientist Description: The Drug Safety... more

Title: Clinical Contract Coordinator in Bridgewater, NJ. Duties: This position supports North America Scientific & Clinical Purchasing with contract coordinating for new contracts... more

Drug Safety Scientist needed for a 6 month position with potential for renewal in S. San Francisco. Drug Safety Scientist (DSS) is responsible for implementing and coordinating... more

Represents Regulatory Affairs on product lifecycle teams by actively contributing to the development and implementation of regulatory strategies. Independently prepares and... more

Medical Sourcing Mngr (6m)-1. Works with the category lead and relevant medical business partners globally to establish and implement category strategy. 2. Identifies, formulates... more

To provide SAS programming support for the Clinical Research Programming Department. ESSENTIAL FUNCTIONS: (Core Responsibilities - See Attachment II) Develop and document programs... more

An professional with experience in negotiating, drafting, revising and implementing contracts. This candidate would also administer the contracts, acting as the liaison between... more

based on the potential exposure to certain health hazards encountered as a result of their job function. Education: A minimum of a Bachelors degree in a scientific discipline is... more

A Clinical Trial Assoicate I is needed for an 18-month contract position at major biotech in Northern California. contract Clinical Trial Associate (cCTA) reports to Clinical... more

This position supports North America Scientific & Clinical Purchasing with contract coordinating for new contracts and change orders including contract planning, preparation, &... more

Description Individual will partner with individuals within Clinical Data Management to provide operational support. Duties include entry of data into vendor work order system,... more

such as biostatistics, biometry, public health or biological sciences) or Bachelor's degree plus three years related job experience, or equivalent experience. Exposure to... more

? Responds to ad hoc safety queries from the Health Authorities, through the responsible RA Manager ? Working with the signaling team, identifies, analyses, assesses, and... more

Provide leadership as a group manager and a statistical expert on a statistical group or a project team within oncology area. For one or more projects, be accountable for all... more

Exciting opportunity to leverage your Database Marketing Specialist expertise with a growing analytics global organization - role can be based in NYC, Mexico City or Brazil!... more

Title: Managing Director, Market Research Location: Chantilly, VA Salary: $130 - $150K + bonus Contact: sbaron@smithhanley.com Our client seeks a senior market research... more

Title: Regulatory Compliance Auditor, Sr. in Menlo Park, CA. Description: 1. 10+ yrs of experience, must have prior exp with Medical Device 2. Exp with European Medical Device... more

Title: Research Analyst/Electrical Engineer Location: Bloomington, IL Full relocation supported by the company Salary Range: TBD NO SPONSORSHIP AVAILABLE AT THIS TIME For more... more

Technical Writer (3m)-Technical Writing role writes, or supports the development of, various technical documents such as: requirements, specifications, test plans, and user... more

Product Manager - Dermatology Chicago Area Develop and implement promotional tactics directed toward dermatology healthcare professionals for the Dermatology professional... more

Pharmaceutical Company looking for a contract Study Data Manager in Montville, NJ. Requirements: BA or equivalent preferred in Natural Sciences, Informatics or Medical... more

Qualifications: Minimum two years Pharmaceutical Industry Regulatory experience. Experience supporting Product Registration Data Management activities for global data in the... more

Individual will partner with individuals within Clinical Data Management to provide operational support. Duties include entry of data into vendor work order system, coordination... more

Bachelors degree with 3 years health sciences or related nursing experience. Must have demonstrated analytical, problem-solving, organizational, and interpersonal skills. Must... more

QA final labeling and promotional materials and create high-quality, accurate submissions to FDA Supports Promotional Review Committee (PRC) Chairs and PRC team members by... more

POSITION DESCRIPTION: Evaluate adverse events involving Neuromodulation products to determine MDR/ADR eligibility. Report MDR/ADR eligible events to the FDA within the MDR/ADR... more

Basic Qualifications: MD, 2+ years experience Drug safety/drug development experience Adverse Event Management Competencies: Understand post-marketing safety, clinical trials and... more

Participate in ongoing comprehensive product/disease area training to serve as Medical Information expert within area of responsibility Ability to communicate on professional... more

Job Title: Regulatory Assistant in South San Francisco, CA. Duties: - QA final labeling and promotional materials and create high-quality, accurate submissions to FDA - Supports... more

Safety Assistant (12m)-Execution of local activities relevant to the management of safety data Primary Responsibilities: - Maintain local documentation as required by legislation... more

Title: Clinical Studies Specialist - A in Northern Suburb of Chicago, IL. Description: - Requires attention to detail. - Administration experience a plus. - Required to file in... more

The Statistical Programmer is responsible for providing significant programming support to the statisticians as part of the contribution towards the completion of statistical... more

Quality Compliance Spec (12m)-Perform Regulatory Compliance Audits as needed: Self Inspections, Supplier, and Third Party Audits Manage audit lifecycle (audit report, CAPA follow... more

preparation of CPP reports to be filed with health authorities Perform quality control on analysis data sets, Spotfire files, and all reports and output Interact with members of... more

Contractor Requirements Skills Needed: - Advanced Excel - Manipulate data, write formulas, and utilize Pivot Tables - Power Point - Create/edit graphs - SAS Programming - Write... more

analytic solutions or consulting company, or health care institution; with at least 3 in a client-facing project management capacity. * Proficiency in analytical tools is required... more

Join a dyanamic and growing health and hygiene solutions companyin NE ... Health, Managed Care or targeting KOL's or health care providers. Having a hands on... more