Clinical Positions

We have many opportunities with our Pharmaceutical clients for clinical professionals.

*Clinical Medical Writers
(Desk top publishing in the creation of regulatory labeling (e.g., package inserts, etc.) for diagnostic (IVD) products. Must be proficient in specific desk top publishing software applications such as Adobe Creative Suite (InDesign, Illustrator) and FrameMaker and software in the Windows environment (Word, Powerpoint, and Excel). Experience required in copyediting and proofing of technical documents. The candidate should have a bachelor's degree in science with a minimum of 2 years experience with regulated scientific documents in a medical field, preferably the pharmaceutical or IVD industry. Position is located in Des Plaines.)

*Clinical Medical Services Specialist - Several positions.
#1 - (ADN, Diploma, or BSN -prepared Registered Nurse, RPh or PharmD required. Must have good verbal communication skills, and clinical experience. Provides medical, pharmaceutical product, and disease-state information to healthcare professionals, consumers and sales representatives in response to verbal and written inquiries in a timely manner. Correctly utilize provide data sources to disseminate accurate medical information, including injection administration assistance, using established information dissemination guidelines. Identifies and communicates adverse events and product complaints to appropriate departments according to established procedures.)
#2 - (Required (must have) RN or Pharmacy license, BSN highly desired. Responsible for processing serious adverse events in the Clinical Safety database. Capable of applying clinical knowledge base to adverse event reporting and assessment. Able to perform the detailed quality assurance of reports in a timely manner to meet regulatory compliance. Microsoft programs and Lotus Notes experience preferred.
#3-(Required- RN or Pharmacy license, BSN Highly Desired: Answer Health Care Professionals' questions regarding adverse events in the Postmarketing database. Consumer questions are addressed regarding package insert related product information. Postmarking Safety is also involved in the ongoing review of reported events as they relate to a drug safety profile, and in responding to ad hoc government agency requests. Good communication/good computer skills necessary. Microsoft programs preferred. Lotus Notes experience required.)

* Clinical Project Manager
(Development of clinical policies, processes and procedures for GPRD and Affiliate clinical teams. Includes responsibilities for SOPs which comply with Global Good Clinical Practices (GCPs).Identify procedures needed as the organization evolves, industry practices change and regulations change. Facilitate SME involvement and partner with Global Project Teams, Regulatory Affairs and Quality Assurance to ensure that GPRD and Affiliate clinical practices are within regulatory and ethical compliance. Manage logistics of document development, review, approval and distribution. Maintain currency in current regulations, policies, and emerging new regulations affecting clinical research to ensure GPRD Clinical systems, processes, procedures and training appropriately reflect current global standards. Perform impact analyses as required by new regulations and standards.)

* Clinical Project Manager, Assistant
(Responsible for supporting three drug studies, works closely with the project teams to investigate and resolve issues. Pharmacist Preferred or Clinical Research Experience with BS degree. Must have great written and verbal communication skills, proficient in MS Project, Excel, Word, and Lotus Notes highly desired.)

* Clinical Medical Reviewer/Safety Reviewer-Several positions
(RN required. BSN preferred. Experience in oncology related field beneficial. Experience in pharma, CRO, or as a coordinator for a physician.)

* Clinical Statistician II - several positions
#1 - (Must have an MS or higher in biostatistics and statistics with at least THREE years experience as a statistician or programmer in a clinical trials environment (Pharma, Hospital or CRO). With GPA’s of least 3.65)
#2 - ( Must have an MS or higher in biostatistics and statistics with minimum ONE year experience as a statistician or programmer in a clinical trials environment (Pharma, Hospital or CRO). GPA's 3.65 or above.)
#3 - Location in NJ.(Candidate must have written SAP (Statistical Analysis Plan) generated analysis and reporting for Phase II - III clinical trials. Strong communication skills so that the clinical trials finding can be communicated to clinicians or person not having statistics background. They should also have either a MS degree with 5 + years experience or PH.D. with 3 + years in the Pharmaceutical Industry.)

* Clinical Application Specialist III
3 TO 5 YEARS OF EXPERIENCE. programming of tables, listings, and graphs for a specified compound project. Responsible for the validation and quality assurance of any output produced for specified projects and contributing to all project management such that timelines are met. responsible for assisting the Project leader with training for junior programming members of the team. Back-up participant on Clinical Project teams representing clinical programming efforts for that clinical team. Prefer candidate with SAS program and clinical experience. BS/MS Preferred.)

LG Associates/Asen Computer Associates is a nationwide provider of clinical and information technology consulting and staffing. Our reputation for providing outstanding service has been proven over the past 30 years of business. We can provide you with an excellent opportunity to enhance your career path. We are looking for professionals with creativity and a strong drive for growth and success. To help you meet your career goals, we offer you the opportunity to work for exciting and growing global corporations. We know what it takes to be successful and we look forward to working with you.

The company offers contract, contract for hire and full time opportunities.
REQUIREMENTS
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