Description

Clinical Development Scientist will be a part of the study specific sub-teams, acting as a primary point-of-contact for questions and inquiries to the study protocol and contents within. This role has primary responsibility for the development of clinical study design, writing various clinical documents such as, but not limited to, clinical study synopsis, clinical study protocol, investigator brochures etc.

Accountability\tKey Responsibilities\t% of Time

Clinical Lead\t

\tLead development of study designs.

\tLead writing of protocols, and amendments, ICFs, and clinical sections of other documents.

\tLead clinical study data review and interpretations

\tLead the preparation and presentation of clinical study data at management meetings.

\tTrack and update the CD deliverables across all clinical studies responsible.

\tRegular maintenance and update of the CD project folders/drives.

Clinical Study Planning Development, Data and Reports\t

\tAuthor study documents such as Protocol Synopses, Protocols, Protocol amendments, Administrative Change letters etc.

\tEnsure trial implementation according to the Study protocol.

\tAuthor and timely review of trial-related documents such as the IBs, ICF, CRFs, CRF Completion Guidelines, Study Execution and Monitoring Plans, Clinical Data Review Plan, Clinical Database specifications, statistical analysis plan, the data management plan, the medical monitoring plan, Clinical Study Report (CSR) etc.

\tRegular and ad-hoc data reviews and interpretation; prepare and present summaries/documentations of these reviews to Indication Lead and Senior Director/Director, clinical development.

\tSupport the development of program-level documents, including, but not limited to, abstract and manuscripts, presentations, and various other internal and external documents and communications as needed.

\tAssist in the review of clinical study entries (clinical trial information and results) for posting to the Endo CTRR (Clinical Trial Registry and Results) database/TPR (Third Party Registry).

\tSupport identifying, contracting and engaging subject matter experts/thought leaders in advisory board meetings, consultancy etc.

Clinical Operations\t

\tParticipation in vendor selection process, specification development, and management/oversight, as needed.

\tDevelop/coordinate study specific training materials for study team, investigational sites, and vendors.

\tEnsure CD participation and presentations at Investigator meetings or similar.

\tOversee & guide Clinical Development Scientists with scientific and data-related queries.

Safety & Efficacy\t

\tEnsure collaboration between Clinical Development Scientists and Clinical Safety Scientists & PVRM for identifying trial-related safety trends, and as needed, generate reports to interpret, analyze and summarize the data and trends.

\tEnsure collaboration between Clinical Development Scientists and statisticians to identify any trial-related efficacy trends, and as needed, generate reports to interpret, analyze and summarize the data and trends.

Additional Skills & Qualifications

•\tAdvanced Scientific degree (PhD/PharmD/Masters degree)

•\tAt least 5 years of experience in clinical development within Industry (pharmaceutical, CRO)

•\tPrevious experience designing and developing phase 1-4 protocols.

•\tGood therapeutic area experience (typically demonstrable with 2 or more years relevant experience).

•\tGood experience in the principles and techniques of data analysis, interpretation and clinical relevance (e.g., ISS, ISE, competitor data, etc.).

•\tData listing review experience.

•\tExperience working on a clinical team.

•\tPrevious project management/clinical operations experience desirable.

•\tLocation: Home office anywhere in the US- must be available during core CST business hours, may need to travel to Endo (in PA) for quarterly/biyearly meetings.

Experience Level

Expert Level

Pay and Benefits

The pay range for this position is $84.00 - $88.94/hr.

Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully remote position.

Application Deadline

This position is anticipated to close on Jun 27, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.