Biotech Jobs in Manama

Operational Study Management for 1 or more studies of moderate complexity generally with responsibility for all study management aspects of assigned studies Accountable for the development of realistic detailed study startup and monitoring plans Accountable for conducting country More...

Enables medical pre-launch and launch preparation across all ex-US affiliates in one out of four respective areas in Oncology: Breast Cancer / Women`s Health, Lung Agnostic Rare Skin (LARS), GI&GU Cancers, Hematology & Hemophilia Coaches local medical teams to drive local o More...

Achieve company sales target by developing new business with existing and new clients Market research and contact prospects through emails and cold calling and face to face approach during conferences or customer visits. Actively and successfully manage the sales process Lead reg More...

Collaborate with regional value evidence teams and global cross-functional teams to plan and coordinate evidence generation activities in accordance with priority setting Understand the needs and pathway in countries towards reimbursement of vaccine Guide the clients regional and More...

Installing and calibrating biomedical machines, equipment, and software. Evaluating the safety, efficiency, and effectiveness of biomedical machines, equipment, and software. Maintaining and repairing biomedical machines and equipment, when needed. Providing technical support, wh More...

Ensure execution of preventive maintenance schedules. Ensure be able to adopt the technology transfer activities. Ensure that all products are manufactured by GMP, company policies & procedures. Report to upper management. Monitor operations and trigger corrective actions.

Ensure that inventory is updated as per physical stocks and proper stock control is maintained. Responsible for ensuring proper execution of stock counts and cycle counts according to the policies. Responsible for ensuring compliance from a data integrity point of view and optimiz More...

Doing the production and QC programming of SDTM datasets, analysis datasets (ADaM), tables, listings, and figures, for multiple clinical trials using SAS software. Integration data across multiple studies or drug programs. Working with minimal supervision under the direction of a More...

Provides regulatory support for country specific Early Access Programs (EAPs). This may also include the preparation of supportive regulatory documents for these programs. Collaborates with project teams and other internal and external key stakeholders as appropriate to ensure effe More...

Conducting health and wellness screenings. Providing immunizations, and other medical services, such as taking blood pressure, temperature measurements, and checking blood sugar levels. Keeping accurate customer records. Ensuring a safe and clean working environment.

. Maintaining and motivating a successful team by recruiting, training, and coaching employees; ensuring a safe, secure, and compliant work environment; providing your team with professional development and growth opportunities. . Within your own statistical programmer team, monitori More...

Create, validate, execute and generate statistical programs consisting of listings, safety and efficacy outputs (analysis datasets, tables, figures) . Create and finalise project or departmental level macros . Create and finalise programming specifications/mock-ups . In accordanc More...

Identifying and meeting customers (HCPs) Reviewing sales performance and developing Marketing plans to achieve objectives. Monitoring and analyzing data and market dynamics to identify competitive advantage. Key accounts and Stakeholders Mapping. Developing regular interactions. More...

Responsible for regulatory affairs activities to assist in regulatory submission, annual reports, registrations and listings. Assure compliance with applicable medical device regulations per jurisdiction, guidance and standards. Assist in creation and maintenance of regulatory files More...

Provide input in protocol development/amendment Review data to ensure concordance across efficacy assessments Perform BILAG and MDAAT grading for each organ system, if applicable. Trains study teams (protocol specific training on efficacy tools). Start-up activities including si More...

Serve on Sponsor Standards and Technology Leadership teams. Consult with clients on sponsor-specific CDISC centric implementation projects. Participate in industry groups focused on the development of standards related initiatives (e.g. CDISC, PhUSE etc.). Author, maintain, imple More...

recruiting, training and managing staff processing prescriptions and dispensing medication ordering and selling medicines and other stock meeting medical representatives managing budgets keeping statistical and financial records preparing publicity materials and displays

Accountable for delivery of global trials within agreed/projected life of trial budget. Ensures accurate trial budget management, updates for scope changes and reconciliation of assigned trials for both Out of Pocket costs and FTE costs Lead the cross-functional Trial Team; Trackin More...

Approves new equipment by conducting tests, ensuring adherence to codes and making modifications. Installs new equipment by establishing, adjusting, calibrating and testing performance. Maintains equipment by completing preventive maintenance schedules, conducting tests and troubl More...

Fulfilling tasks set out by supervisors from several departments. Attending meetings and taking minutes. Performing research at a supervisor's request. Updating social media platforms and writing copy for posts. Creating images for social media posts.