Clinical Research Associate

At PharmaGen, we value diversity and believe that a diverse workforce contributes to our success. We offer a competitive salary, comprehensive benefits, and opportunities for professional growth and development. If you are passionate about making a difference in the lives of patients and have a strong background in clinical research, we encourage you to apply for the position of Clinical Research Associate.

Position: Clinical Research Associate

Company: PharmaGen

Location: Farafenni, Gambia

Type: Full-time

Salary: DOE

About the Company: PharmaGen is a leading clinical research organization dedicated to improving the lives of patients by conducting high-quality clinical trials. With a focus on innovative and evidence-based solutions, we partner with pharmaceutical, biotechnology, and medical device companies to bring new treatments to the market. Our team of experienced researchers, physicians, and support staff work together to ensure the successful completion of each trial.

Job Overview: We are seeking a highly motivated and detail-oriented Clinical Research Associate to join our dynamic team. As a Clinical Research Associate, you will be responsible for monitoring and managing clinical trials to ensure the safety and efficacy of investigational drugs and medical devices. You will work closely with the research team, investigators, and study participants to ensure that all aspects of the trial are conducted in compliance with regulatory guidelines and company protocols.

Key Responsibilities:

• Conduct pre-study, initiation, routine, and closeout visits at clinical trial sites to ensure compliance with study protocols, Good Clinical Practice (GCP), and applicable regulatory guidelines.
• Develop and maintain strong relationships with investigators, site staff, and study participants to facilitate successful study execution.
• Perform source document verification, data collection, and data entry to ensure accurate and complete data is collected and recorded.
• Monitor and review study progress, including enrollment rates, data quality, and protocol deviations, and provide regular updates to the project team.
• Create and maintain study documents, including study binders, source documents, and regulatory documents.
• Assist with study start-up activities, including site selection, contract and budget negotiation, and ethics committee submissions.
• Participate in investigator meetings, training sessions, and other study-related activities.
• Ensure compliance with all applicable regulatory requirements and company policies and procedures.

Qualifications:

• Bachelor's degree in a health-related field, such as nursing, pharmacy, or biological sciences.
• Minimum of 2-3 years of experience as a Clinical Research Associate in the pharmaceutical or biotechnology industry.
• Strong knowledge of GCP, FDA regulations, and ICH guidelines.
• Excellent organizational, communication, and interpersonal skills.
• Proven ability to work independently and in a team environment.
• Strong attention to detail and ability to prioritize tasks effectively.
• Willingness to travel up to 70% of the time to various study sites.
• Proficiency in Microsoft Office Suite and electronic data capture systems.

Join our team and help us bring new treatments to those in need.