General Manager at African Clinical Research Limited(ACR)

African Clinical Research Limited (ACR) is a wholly indigenous Site Monitoring Organization founded with the goal of bringing health to all Africans through the latest advances in Clinical Research by being exceptionally responsive to the needs of the medical community and to exceed expectations in every aspect of the services we provide. We have a solid team of research professionals (Physicians, Coordinators etc.) dedicated to our goal.

We are recruiting to fill the position below:

Job Position: General Manager
Job Location: Ondo

Job Description

• An exciting new job opportunity has opened for a suitable candidate to develop, implement and deliver top-notch managerial relationship and attitude for African Clinical Research Limited. A passion for technology and project delivery focused is required.

Job Responsibilities

• Oversees day-to-day business operations
• Provides leadership to all levels of the organization
• Communicates and embody the company’s vision and values
• Builds up the company by interviewing, hiring, and mentoring new talent
• Defines and implement policies and performance standards
• Evaluates employee performance and provide additional coaching and support as needed
• Assesses departmental and company performance and devises plans for improvement
• Manages profit and loss statements and accounts for costs and revenues
• Allocates budget resources for supplies, equipment, marketing, and personnel
• Supports clinical research team (physicians, nurses, etc.) in research efforts by facilitating the protocol approval process and maintaining documentation of regulatory compliance throughout the trial’s duration for research studies involving human subjects.
• Establishes and maintains processes and also monitors practices to ensure regulatory documentation involving clinical trials complies with Institutional Review Board (IRB) policies, procedures, and regulations.
• Manages identified issues and provides feedback to leadership regarding resolution.
• Disseminates information and participates in training.
• Provides direction and feedback to the research team to ensure awareness of business practices and quality standards.
• Documents any exceptions to compliance standards.
• Manages new submissions and continuing review activities.
• Reviews initial submissions to determine the review category and action to be taken.
• Completes submission applications, and other required documentation prepares protocol specific forms for submission to various review committees, including internal scientific review boards, the IRB and sponsoring entities.
• Serves as lead contact for each assigned trial, maintains records and corresponds with all parties involved (institutional, federal, pharmaceutical).
• Completes protocol renewal applications, amends applications and maintains the record of all adverse event reports.
• Attends research team meetings and reports on regulatory issues.
• Responsible for administrative duties corresponding to budgets and contracts.
• Performs related responsibilities as required.

Job Requirements
Education:

• B. Pharm/MBBS. MBA preferred.

Knowledge, Skills & Experience:

• Market knowledge
• English language fluency
• Oral, written & presentation skills
• Ability to build strong relationships
• General sales skills, including need identification, questioning, listening, negotiation and closing.
• Strategy development skills
• Motivated, dynamic & industrious with “can-do” attitude.
• Personable & professional appearance
• Good commercial acumen.
• Past managerial experience required.