GlaxoSmithKline is a world leader in Consumer and Healthcare products with a strong marketing orientation and a wide range of products. Career opportunities exist in the following roles: Clinical Research Associate CLINICAL RESEARCH ASSOCIATE The Job Reporting to the Bio Clinical Operations Manager and Head of Medical, the role has the responsibility to: • Liaise with Medical Advisor(s)/ Director and Clinical Operation team to identify suitable investigators for clinical trials. • Assess investigator’s staff and facilities (working areas, lab, temperature controlled storage) • Apply a high standard of monitoring, source document verification and compliance with SOPs, ICH GCP and study protocol to ensure high quality data which is acceptable for regulatory submissions. • Coordinate all clinical research activities on site as the reference person for the sponsor. • Ensure that all Serious Adverse Events are reviewed & reported in compliance with SOPs, ICH GCP and local regulatory requirements. • Track & achieve project milestones and timelines • Assist the Medical Advisor / Clinical Operations Manager to draw up a mutually acceptable and accurate financial/study agreement to ensure optimum management of local trial budgets. • Take an active role in process development and implementation, in sharing best practices, especially in a regional champion’s role. • Cultivate and maintain strong working relationships and communication with investigators and GSK staff. • Ensure proper management /storage/ availability of clinical trial supplies, vaccines and biological samples at site, • Ensure site staff is appropriately trained according to ICH-GCP/ SOP, SOPs and In liaison with the Regional Training Manager.

GlaxoSmithKline is a world leader in Consumer and Healthcare products with a strong marketing orientation and a wide range of products. Career opportunities exist in the following roles: Clinical Research Associate CLINICAL RESEARCH ASSOCIATE The Job Reporting to the Bio Clinical Operations Manager and Head of Medical, the role has the responsibility to: • Liaise with Medical Advisor(s)/ Director and Clinical Operation team to identify suitable investigators for clinical trials

Golden Pasta Company is a subsidiary of Flour Mills of Nigeria and a leading pasta producer in the Nigerian Market. Golden Pasta is recruiting for Technical Manager Position: TECHNICAL MANAGER The Job • Responsible for research & development initiatives for process and products. Qualification • BSc Engineering in Food Technology. Experience • At least 10 years experience in R&D in a Food processing (Noodles) company. Method of Application Interested applicants should forward their detailed resume with a passport photographs to: info@goldenpastang.com (Please note that only shortlisted candidates will be contacted) Deadline: 7th September 2010 |

JOIN OUR TEAM As part of our current drive at strengthening our process and providing leading edge support for our operations, we are soliciting from suitably qualified candidates to fill the positions below in our structured organization: RESEARCH AND DEVELOPMENT OFFICER (PROCESS) REF: HR/ADM/003 KEY RESPONSIBILITIES: Successful candidates would be assigned responsibilities in the underlisted functional arrears among others: Assisting in new product development and line improvement programs Assisting in providing research information and idea generation Assisting in work study of processes Assisting in ensuring stability in studies of new / existing products QUALIFICATION AND EXPERIENCE Our ideal candidate should: Possess a minimum of BSC or HND Chemistry, industrial Chemistry or Biochemistry Have five (5) years cognate work experience in research in a structured Food and beverages company Have intergrity and ability to work under pressure Not be more than 35 years old OFFICE ASSISTANT REF: HR/ADM/004 KEY RESPONSIBILITIES Successful candidates would be responsible to the secretary to the Managing Director Supporting the Managing Director’s secretary in office Administration at all times Typing of documents promptly without errors, confidently filings of correspondences and dispatch of mails/documentation in an effective manner Granting confidential treatment to all information accessed by virtue of the position QUALIFICATION AND EXPERIENCE Our ideal candidate should: Possess a minimum of OND in secretariat Administration Have acquired at least three (3) years cognate in a structured organization Must be computer literate and proficient in the use of MS Word, Excel and Power Point Must posses excellent communication and good interpersonal skill Must be very hard working Be between 25 – 30 years old REMUNERATION: The remuneration attached to the position are very attractive and comparable to industry standard HOW TO APPLY Interested candidates should forward their hand written applications, photocopies of credentials and detailed curriculum vitae, providing full details of contact address (not P.O. BOX) and day time telephone number to: THE HUMAN RESOURCES MANAGER P.M.B 21410, IKEJA – LAGOS All application should be submitted not later than two weeks from the date of publication. | WordPress Auto Translator

Tavia Technologies is an experienced technology company offering Web, Wireless & Business Intelligence services. They are recruiting for the following position: Support Analyst (Business Intelligence) Support Analyst (Business Intelligence) The desired candidate for the Support Analyst (BI) role must be able to ensure the goals of the client with respect to data/information management are met. Responsibilities Clear understanding of source and target structures. Building cubes and reports that take advantage of Dimensional Modelling capabilities. Knowledge and experience of business intelligence applications like Hyperion, Cognos and Business Objects

EXCITING CAREER OPPORTUNITY IN MULTINATIONAL MANUFACTURING AND SALES ORGANIZATION. CLINICAL RESEARCH ASSOCIATE THE JOB: Reporting to the Bio Clinical Operations Manager and Head of Medical, the role has the responsibility to: • Liaise with Medical Advisor(s)/Director and Clinical Operation team to identify suitable investigators for clinical trials • Assess investigator’s staff and facilities (working areas, lab, temperature controlled storage) • Apply a high standard of monitoring, source document verification and compliance with SOPs, ICH GCp and study protocol to ensure high quality data which is acceptable for regulatory submissions • Coordinate all serious adverse events are reviewed & reported in compliance with SOPs, ICH GCP and local regulatory requirements • Track & achieve project milestones and timelines • Assist the medical advisor/clinical operations manager to draw up a mutually acceptable and accurate finance/study agreement to ensure optimum management of local trial budgets • Take an active role in process development and implementation, in sharing best practices, especially in a regional champion’s role • Cultivate and maintain strong working relationships and communication with investigators and GSK staff • Ensure proper management / storage/availability of clinical trial suppliers, vaccines and biological samples at site • Ensure site staff is appropriately trained according to ICH-GCP/SOP,SOPs and liaison with the regional training manager • Co-ordinate with Investigators and Medical Director/ Central GSM the preparation for internal and external Audits • Answer questions, propse specific action and ensure their implementation in his/her activity area THE PERSON The ideal candidate must have a very good health science degree from a reputable university with a minimum of 3 years post NYSC. Post graduate qualification(s) are an added advantage