Senior Clinical Research Scientist (Pharmacology)

Placements24; East London; Hybrid; ZAR 1,200,000 - 1,800,000; Full time

Benefits offered by this job

Health, dental, and vision insurance

Professional training and conferences

Flexible remote/hybrid work

Job summary

Placements24 in East London, Eastern Cape, is seeking a Senior Clinical Research Scientist with pharmacology specialization to design, oversee, and optimize clinical trials from early to late-phase studies, ensuring robust pharmacology assessments and regulatory compliance.

You will lead trial design and execution, manage relationships with investigators, prepare reports and submissions, and mentor junior researchers in a remote or hybrid capacity to support innovative drug development.

Qualifications

• Ph.D. or Pharm.D. in Pharmacology, Pharmacy, or related life science.
• Minimum of 6 years of experience in clinical research, with focus on drug development and pharmacology.
• Proven experience designing and managing Phase I–IV clinical trials.
• In-depth knowledge of drug metabolism, pharmacokinetics and pharmacodynamics.
• Familiarity with regulatory requirements (FDA, EMA) and GCP guidelines.
• Excellent analytical, critical thinking and problem-solving skills.
• Strong written and verbal communication with ability to present complex scientific information clearly.

Responsibilities

• Design clinical trial protocols in alignment with therapeutic area strategies and regulatory guidelines.
• Oversee the execution of clinical trials, ensuring adherence to GCP and ethical standards.
• Analyze and interpret complex clinical data, including PK/PD assessments.
• Develop and manage relationships with clinical investigators, site staff, and external collaborators.
• Prepare scientific documentation, including study reports, manuscripts, and regulatory submissions.
• Contribute to drug candidate strategy and lifecycle management.
• Stay abreast of advancements in pharmacology, clinical research, and regulatory affairs.
• Present study findings at scientific meetings and internal strategy sessions.
• Mentor junior research staff and contribute to scientific excellence of the team.

Skills

Clinical trial design

PK/PD analysis

Regulatory knowledge

Scientific communication

Mentoring

Education

Ph.D. or Pharm.D. in Pharmacology/Pharmacy or related life science

Job description

About the Role

Our client, a globally recognized pharmaceutical research company, is seeking a highly motivated and experienced Senior Clinical Research Scientist with a specialization in pharmacology to join their dynamic team in East London, Eastern Cape . This crucial role will involve designing, implementing, and overseeing clinical trials focused on evaluating the efficacy and safety of novel therapeutic agents. You will play a key role in drug development, from early-phase studies to late-stage trials, contributing significantly to bringing life-saving treatments to patients. The ideal candidate will possess a deep understanding of pharmacology, clinical trial methodologies, and regulatory requirements, along with a passion for scientific innovation and a commitment to patient well-being. This is an exceptional opportunity to contribute to cutting-edge pharmaceutical research.

Key Responsibilities

• Design clinical trial protocols in alignment with therapeutic area strategies and regulatory guidelines.
• Oversee the execution of clinical trials, ensuring adherence to Good Clinical Practice (GCP) and ethical standards.
• Analyze and interpret complex clinical data, including pharmacokinetic and pharmacodynamic (PK/PD) assessments.
• Develop and manage relationships with clinical investigators, site staff, and external collaborators.
• Prepare scientific documentation, including study reports, manuscripts for publication, and regulatory submissions.
• Contribute to the development of drug candidate strategy and lifecycle management.
• Stay abreast of the latest advancements in pharmacology, clinical research, and regulatory affairs.
• Present study findings at scientific meetings and internal strategy sessions.
• Mentor junior research staff and contribute to the scientific excellence of the team.

Requirements

• Ph.D. or Pharm.D. in Pharmacology, Pharmacy, or a related life science discipline.
• Minimum of 6 years of experience in clinical research, with a strong focus on drug development and pharmacology.
• Proven experience in designing and managing Phase I-IV clinical trials.
• In-depth knowledge of drug metabolism, pharmacokinetics, and pharmacodynamics.
• Familiarity with regulatory requirements (e.g., FDA, EMA) and GCP guidelines.
• Excellent analytical, critical thinking, and problem-solving skills.
• Strong written and verbal communication skills, with the ability to present complex scientific information clearly.
• Ability to work effectively in a remote or hybrid capacity, contributing to a team based near East London, Eastern Cape .

Benefits

• Our client offers a highly competitive salary and a comprehensive benefits package, including health, dental, and vision insurance, as well as a generous retirement savings plan.
• We are dedicated to supporting our employees' professional growth through access to ongoing training, educational opportunities, and attendance at leading scientific conferences.
• This role provides a stimulating and collaborative work environment focused on advancing pharmaceutical innovation.
• The flexibility of remote work enhances work-life balance for our valued team members.