Requirements:
Education and Experience Requirements:
High / Secondary school diploma or equivalent and relevant formal academic / vocational qualification.
Bachelor's degree preferred.
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 1 year).
In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
Knowledge, Skills and Abilities:
Ability to work in a team or independently as required
Good organizational skills and strong attention to detail, with proven ability to handle multiple tasks efficiently and effectively
Demonstrated ability to effectively analyze project-specific data/systems to ensure accuracy and efficiency
Strong customer focus
Flexibility to reprioritize workload to meet changing project timelines
Demonstrated ability to attain and maintain a good working knowledge of applicable Country Regulations, ICH Good Clinical Practices, and organization/Client SOPs and WPDs for all non-clinical/clinical aspects of project implementation, execution and closeout
Good English language and grammar skills and proficient local language skills as needed
Good computer skills, proficient in MS Office (Word, Excel, and PowerPoint) and ability to obtain knowledge and master all clinical trial database systems
Ability to successfully complete the organizations clinical training program
Self-motivated, positive attitude and good interpersonal skills
Effective oral and written communication skills
Good interpersonal skills
Essential judgment and decision-making skills
Capable of accurately following project work instructions
Good negotiation skills
Independent thinker
Ability to manage risk and perform risk escalation appropriately

Requirements:
Requirements:

B.A. / M.A. in Brain Sciences, Health/Medical studies.

At least 1-2 years of experience with medical imaging/ annotation/ working with medical data a records.

Demonstrable in-depth understanding of human anatomy.

Medical research oriented.

Attention to details.

Ability to prioritize effectively.

Curious, proactive, and continuous learner with strong interpersonal and collaborative skills.

Strong technical skills, fast learner.

People person, team player.

Requirements:
English - native language a must.
2+ years of hands-on experience in academic or scientific writing, preferably in a medical, clinical, or biotech environment.
Proven publication of more than 10 academic papers.
Demonstrated experience publishing in peer-reviewed journals, as lead or contributing author.
Strong understanding of clinical research methodologies, data interpretation, and ethical publishing standards.
Ability to work independently and manage multiple writing projects simultaneously.
Excellent attention to detail, with strong editing and proofreading skills.
Academic background in life sciences, biomedical engineering, clinical research, or related field.
Knowledge of regulatory and clinical frameworks (e.g., MDR, FDA, GCP) - an advantage.