Senior Clinical Research Associate at PSI CRO

, West Coast Division, The Gambia -

Full Time

Start Date

Immediate

Expiry Date

21 May, 26

Salary

0.0

Posted On

20 Feb, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Onsite Monitoring, Clinical Research, Study Startup, CRF Review, Source Document Verification, Query Resolution, Site Communication, Timeline Management, Quality Control, Compliance Monitoring, Feasibility Research, Regulatory Submissions, Oncology Trials, Radiopharmaceuticals, MS Office, Multitasking

Industry

Pharmaceutical Manufacturing

Description

Company Description We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,800 driven, dedicated and passionate individuals. We work on the front-line of medical science, changing lives, and bringing new medicines to those who need them. If you feel it is time to make your skills and knowledge visible within a growing company with true focus on its people, then PSI is the right choice for you. Job Description As a Senior Clinical Research Associate you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. You will focus on subjects’ rights, safety and well-being and quality of data compliance. You will: Conduct and report all types of onsite monitoring visits Be involved in study startup (if applicable) Perform CRF review, source document verification and query resolution Be responsible for site communication and management Supervise study activities, timelines, and schedules on the country level Be a point of contact for in-house support services and vendors Be involved in quality control, such as compliance monitoring and reports review Participate in feasibility research Support regulatory team in preparing documents for study submissions Qualifications College/University degree in Life Sciences or an equivalent combination of education, training & experience Independent on-site monitoring experience in the USA (5 years minimum) Experience in all types of monitoring visits in Phase I-III Participation in clinical projects as a Senior Monitor Experience monitoring complex Oncology trials required; experience with radiopharmaceuticals and/or breast cancer preferred Experience monitoring GI studies (IBD, Chron's, UC) is preferred. Full working proficiency in English Proficiency in MS Office applications Ability to plan, multitask and work in a dynamic team environment Communication, collaboration, and problem-solving skills Ability to travel up to 80% Valid driver’s license (if applicable) Additional Information Advance your career in clinical research and lead challenging full-service projects on the country/regional level while growing with a rapid company, that puts its people first! You will get hands-on involvement in every aspect of the study. For this position, PSI is not hiring individuals who require work visa for employment or continued employment now or anytime in the future.

Responsibilities

The Senior Clinical Research Associate will manage communication with project stakeholders to ensure clinical research projects meet timelines, targets, and standards across various therapeutic indications. Responsibilities include conducting all types of onsite monitoring visits, managing site relationships, and ensuring subject rights, safety, and data quality compliance.