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Senior Biotech & Pharma Contracts Consultant TaktiKa Consulting Raleigh-Durham, NC Job Details Part-time | Full-time | Contract $150 - $175 an hour 1 day ago Qualifications Contract documentation review Contract review Law Contract law compliance support experience Team leadership Regulatory compliance Contract interpretation Legal risk management Contract management experience in healthcare Business consulting GDPR compliance expertise Team development Policy & process development Contract drafting Continuous improvement Legal drafting Client management Mentoring Negotiating purchasing contracts Vendor contract management Legal client consultation experience

Full Job Description Senior Life Sciences Contracts & Client Success Lead Location:

Remote (U.S. Preferred)

Type:

Part-Time Contract — approximately 15 hours/week initially, with opportunity to expand

Compensation:

$150-$175/hour, commensurate with experience

Reports To:

Founder & CEO

PLEASE READ BEFORE APPLYING WE ARE ONLY CONSIDERING CANDIDATES WITH 7+ YEARS OF EXPERIENCE INDEPENDENTLY REVIEWING AND NEGOTIATING CONTRACTS FOR BIOTECHNOLOGY AND/OR PHARMACEUTICAL COMPANIES. THIS IS A LEGAL/CONTRACTING ROLE

—

NOT A CLINICAL OPERATIONS OR CLINICAL TRIAL MANAGEMENT ROLE.

Candidates must have deep, hands-on experience negotiating sophisticated biotech/pharma agreements. Experience working with contracts as part of a clinical operations role, without substantial independent contract negotiation responsibility, does not meet the requirements for this position. About TaktiKa Consulting TaktiKa Consulting is a boutique consulting firm specializing in contract management, legal operations, contracting process optimization, and CLM support for biotechnology, life sciences, and high-growth companies. We serve as an extension of our clients' legal and contracting teams, providing sophisticated contract negotiation and practical, business-focused contracting support. Position Overview We are seeking a highly experienced life sciences contracts professional who can independently review, redline, negotiate, and advise on complex biotech and pharmaceutical agreements. This is not an administrative contracts role. The successful candidate must be comfortable owning negotiations directly with sophisticated counterparties and advising clients on legal, business, operational, privacy, and compliance risk. The role will also serve as a senior client success lead—managing client relationships, mentoring team members, overseeing quality, and acting as a trusted extension of TaktiKa's Founder & CEO. Key ResponsibilitiesLife Sciences Contract Negotiation Independently draft, review, redline, negotiate, and advise on agreements including: Clinical Trial Agreements (CTAs) CRO MSAs and Statements of Work CMO/CDMO and manufacturing agreements MSAs and commercial agreements Consulting agreements Vendor and supplier agreements SaaS and technology agreements Data Processing Agreements (DPAs) Quality Agreements CDAs/NDAs Work Orders, Amendments, and Change Orders Advise clients and negotiate provisions involving: Indemnification and limitation of liability Intellectual property and licensing Confidentiality Regulatory and clinical research obligations Manufacturing and supply-chain risk Data security and privacy Audit rights Insurance Service levels Financial terms, including FX, inflation, advances, and prepayments Identify material risks and recommend practical solutions aligned with client business objectives and risk tolerance. Privacy & Data Protection Provide practical contracting expertise involving: DPAs and privacy provisions Standard Contractual Clauses (SCCs) GDPR and UK GDPR International data transfers Vendor privacy and security exhibits Data retention, deletion, security, and breach notification Candidates should understand SCC module selection, including Controller-to-Controller, Controller-to-Processor, Processor-to-Processor, and Processor-to-Controller transfers. Client Success & Leadership Serve as a senior point of contact and trusted advisor for assigned clients.

Responsibilities include:

Managing priorities across multiple client engagements Maintaining high-quality, timely contract delivery Advising client stakeholders on contracting strategy and risk Proactively identifying issues and opportunities Building strong relationships with legal, executive, procurement, clinical, and business stakeholders Supporting client satisfaction and retention Escalating material issues appropriately Team Leadership Mentor Contracts Associates and other team members on: Contract interpretation and risk assessment Negotiation strategy Client communications Contracting processes and best practices Support TaktiKa's Founder & CEO with client delivery, resource planning, quality control, training, and development of scalable contracting practices. Required Qualifications 7+ years independently reviewing and negotiating contracts for biotechnology and/or pharmaceutical companies Deep, hands-on experience negotiating sophisticated life sciences agreements Demonstrated experience with CTAs, CRO MSAs/SOWs, CMO/CDMO agreements, commercial MSAs, vendor agreements, and DPAs Ability to independently lead negotiations with sophisticated counterparties Practical knowledge of GDPR, SCCs, and international data transfers Strong contract drafting, redlining, issue-spotting, and risk-assessment skills Strong executive presence and client-facing communication skills Ability to manage multiple clients and competing priorities Experience mentoring or guiding junior contracts professionals Candidates whose experience is primarily in clinical operations, clinical trial management, study management, or contract administration without substantial independent contract negotiation experience will not be considered. Preferred Qualifications JD, Paralegal Certificate, or equivalent depth of contracts/legal experience CIPP/US, CIPP/E, CIPM, or similar privacy certification Consulting experience supporting multiple organizations simultaneously Experience supporting venture-backed and high-growth biotech companies Why Join TaktiKa? Work directly with the Founder & CEO Advise innovative biotech and life sciences companies Work on sophisticated, varied contracting matters across multiple organizations Flexible remote environment Significant autonomy and client visibility Opportunity to help shape the practices and growth of an established boutique consulting firm

Pay:

$150.00 - $175.00 per hour Application Question(s): Describe your experience independently reviewing, redlining, and negotiating Clinical Trial Agreements (CTAs), CRO MSAs, CRO SOWs, and manufacturing-related agreements. Which side of the transaction did you primarily represent? Describe your experience negotiating Data Processing Agreements (DPAs), GDPR provisions, and Standard Contractual Clauses (SCCs). Please include examples of the SCC modules you have worked with and the transfer scenarios involved. What is the single contract clause you negotiate most aggressively in CRO MSAs and why? What is the single contract clause you negotiate most aggressively in

CMO/CDMO

MSAs and why? Please attach a redlined contract that you personally negotiated (with all confidential information removed). We are evaluating drafting and negotiation style, not company information. For the finalists for this position, you will do a 30 min live test where you are given a

CTA, CRO

MSA or CRO SOW, and you walk me through changes you would make in five most important clauses and why. Do you agree to do this?

Work Location:

Remote